USRE33820E - Preparation of alkoxy maleic anhydrides - Google Patents

Preparation of alkoxy maleic anhydrides Download PDF

Info

Publication number
USRE33820E
USRE33820E US07/592,847 US59284790A USRE33820E US RE33820 E USRE33820 E US RE33820E US 59284790 A US59284790 A US 59284790A US RE33820 E USRE33820 E US RE33820E
Authority
US
United States
Prior art keywords
alkyl
alkenyl
haloalkyl
alkoxy
haloalkenyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US07/592,847
Inventor
Rainer Becker
Wolfgang Rohr
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Application granted granted Critical
Publication of USRE33820E publication Critical patent/USRE33820E/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/44—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
    • C07D207/444—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
    • C07D207/456—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40—Unsaturated compounds
    • C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups

Definitions

  • the present invention relates to novel alkoxysubstituted maleimides of the formula ##STR3## where R 1 is hydrogen, C 1 -C 8 -alkyl, C 2 -C 8 -alkenyl, phenyl or phenylalkyl, and the organic radicals may furthermore carry inert substituents, and R 2 and R 3 are each C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 1 -C 4 -haloalkyl or C 2 -C 4 -haloalkenyl, and novel alkoxy-substituted maleic anhydrides of the formula II ##STR4## where R 2 is C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 1 -C 4 -haloalkyl or C 2 -C 4 -haloalkenyl and Z is hydrogen, halogen or a radical OR 3 , where R 3 is C 1 -
  • the present invention furthermore relates to the preparation of the compounds I and II and their use as graft monomers in graft polymers based on polyphenylene ethers.
  • the second halogen atom can be exchanged only using phenolates (cf. J. Org. Chem. 37 (1972), 3637-3645). Dialkoxymaleimides and accordingly also dialkoxymaleic anhydrides are thus not obtainable in this way.
  • alkoxy-substituted maleimides and maleic anhydrides are generally mentioned in various publications, for example in German Laid-Open Applications DOS 1,940,370, DOS 1,936,127 DOS 2,023,077 and DOS 3,217,658, European Pat. No. 19,296 and U.S. Pat. No. 3,816,451
  • no publication contains a characterization of the novel alkoxy-substituted compounds or experimental data on the alleged preparation. It must therefore be assumed that these compounds are purely speculative and have thus not been made available in practice.
  • radicals R 1 are hydrogen and C 1 -C 8 -alkyl, in particular C 1 -C 4 -alkyl.
  • C 2 -C 8 -alkenyl, phenyl and phenylalkyl are also suitable.
  • the stated radicals may furthermore carry substituents which are inert under the reaction conditions, such as alkyl, alkoxy, haloalkyl, haloalkoxy, preferably of 1 to 4 carbon atoms, halogen, e.g. chlorine, bromine or fluorine, nitro or cyano.
  • radicals may be mentioned as examples: hydrogen, methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, hexyl, heptyl, octyl, propargyl, chloroallyl, methoxymethyl, methoxyethyl, phenoxyethyl, phenyl, benzyl, phenylethyl, phenylpropyl and phenylbutyl, where the phenyl group in each case may be substituted by, for example, halogen, such as fluorine, chlorine or bromine, alkoxy, such as methoxy or ethoxy, haloalkoxy, such as fluoromethoxy, difluoromethoxy or trifluoromethoxy, alkyl, such as methyl, ethyl or propyl, or haloalkyl, such as trifluoromethyl.
  • R 2 and R 3 in the compounds I and II are straight-chain or branched, unsubstituted or halogen-substituted alkyl radicals of 1 to 4 carbon atoms, e.g. methyl, ethyl, propyl, isopropyl, butyl or trifluoromethyl. Furthermore, R 2 and R 3 may each be C 2 -C 4 -alkenyl or haloalkenyl. Halogen substituents are, in particular, fluorine, chlorine or bromine.
  • dialkoxy-substituted maleic anhydrides II monoalkoxy-substituted maleic anhydrides and 3-halo-4-alkoxymaleic anhydrides are also of interest, halogen being, in particular, chlorine or bromine.
  • novel maleic acid derivatives can be prepared starting from a dihydroaryliminopyrrole of the formula III ##STR6## where R 2 and Z have the meanings stated in claim 2 and Ar is unsubstituted or substituted aryl, as a key substance.
  • Acidic hydrolysis of III gives the maleimides Ia, which can be converted to the N-alkyl-substituted maleimide in a conventional manner by deprotonation and reaction with an alkylating agent R 1 -Y.
  • Alkaline hydrolysis of Ia and subsequent acidic cyclization by a conventional method give the desired alkoxy-substituted maleic anhydrides II.
  • N-alkyl- or N-alkylphenyl-substituted maleimides may in turn be converted to N-alkyl- or N-alkylphenyl-substituted maleimides by reaction with primary amines R 1 NH 2 , or to N-phenyl-substituted maleimides by reaction with aniline or a substituted aniline.
  • the key substance III is readily obtainable starting from pyridazinones.
  • the aryl radical in III is, for example, phenyl or naphthyl, preferably phenyl. These radicals may carry up to 3 identical or different substituents selected from the group consisting of cyano, halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -haloalkyl and C 1 -C 4 -haloalkoxy.
  • substituted aryl radicals are phenyl, ⁇ -naphthyl, ⁇ -naphthyl, fluorophenyl, difluorophenyl, chlorophenyl, dichlorophenyl, bromophenyl, dibromophenyl, trichlorophenyl, trifluoromethylphenyl, difluoromethylphenyl, methoxyphenyl, ethoxyphenyl, isopropoxyphenyl, tolyl, difluoromethoxyophenyl, trifluoromethoxyphenyl, tetrafluoroethoxyphenyl and cyanophenyl.
  • These phenyl radicals carry the substituents in the 2-, 3-, 4-, 2,4-, 3,4-, 3,5- or 2,4,6-position.
  • the acidic hydrolysis of III is advantageously carried out in the presence of an aqueous acid, for example a mineral acid, such as hydrochloric acid, sulfuric acid or phosphoric acid.
  • a mineral acid such as hydrochloric acid, sulfuric acid or phosphoric acid.
  • other suitable acids are strong organic acids, such as formic acid or acetic acid.
  • the amount of acid is from 10 to 0.1, in particular from 3 to 1, moles per mole of dihydroaryliminopyrrole III.
  • the hydrolysis can be carried out in the presence of an organic solvent, such as low molecular weight alcohols or ethers, e.g. tetrahydrofuran, diethyl ether, methanol or ethanol.
  • the temperature is not particularly critical and may be from 0° to 100° C., preferably from 20° to 50° C. Depending on the reaction temperature, the hydrolysis is complete in the course of a few hours, for example from 1 to 30 hours. At temperatures below 20° C., longer reaction times are required.
  • the maleimides Ia are isolated in a conventional manner, for example by extraction or by filtering off the solid products and if necessary purifying them by recrystallization.
  • the conversion of the maleimides Ia to the N-alkyl- or N-alkenyl-substituted compounds is effected in a conventional manner by deprotonating the imides Ia by means of a base and then reacting the product with an alkylating agent.
  • suitable bases are alkali metal hydroxides, alkaline earth metal hydroxides and alkali metal alcoholates, such as sodium hydroxide, potassium hydroxide, magnesium hydroxide, sodium methylate, potassium ethylate or sodium ethylate.
  • the conventional compounds such as alkyl halides, in particular chlorides, bromides or iodides, alkyl sulfates, alkyl tosylates or alkyl mesylates, can be used as the alkylating agents R 1 -Y.
  • the alkylation is carried out in a conventional manner, so that further description is unnecessary.
  • the preparation of the maleic anhydrides II is carried out by alkaline hydrolysis of the maleimides Ia and cyclization of the maleic acid dianion, formed as an intermediate, in the presence of an acid. If ncessary, the reaction can be carried out in the presence of a water-soluble organic solvent, for example a low molecular weight alcohol or ether.
  • Suitable bases are alkali metal or alkaline earth metal hydroxides or carbonates, e.g. sodium hydroxide, sodium carbonate, potassium hydroxide, potassium carbonate or calcium hydroxide. The amount of base is in general from 1 to 3 equivalents, based on maleimide Ia.
  • the hydrolysis can be carried out at from 0° to 100° C., in particular from 20° to 50° C.
  • the reaction mixture is acidified and the anhydride formed can be isolated in a conventional manner, for example by extraction or by separating it off by filtration.
  • the conversion of the anhydrides II into maleimides can be carried out in a conventional manner by reacting the anhydrides II with primary amines R 1 NH 2 , where R 1 has the meanings stated in claim 1.
  • the reaction can be carried out, for example, as described in German Laid-Open Application DOS 3,222,152, so that further description is unnecessary.
  • novel maleimides I and maleic anhydrides II can be used as monomer components is polymeric systems, in particular as graft monomers in graft polymers based on polyphenylene ethers, with the result that particularly good melt flow in combination with little intrinsic color of the graft polymer is obtained.
  • the graft polymers can be prepared in principle as described in the German Laid-Open Application 3,540,119 or 3,621,207 or in contemporaneous application 37 15 343.9.
  • novel compounds I and II can be used as intermediates in organic syntheses, for example for the preparation of dyes, drugs or crop protection agents.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyrrole Compounds (AREA)
  • Indole Compounds (AREA)
  • Furan Compounds (AREA)
  • Graft Or Block Polymers (AREA)

Abstract

The invention relates to novel alkoxy substituted maleimides of the formula ##STR1## where R1 is hydrogen, C1 -C8 -alkyl, C2 -C8 -alkenyl, phenyl or phenylalkyl, and the organic radicals may furthermore carry inert substituents, and R2 and R3 are each C1 -C4 -alkyl, C2 -C4 -alkenyl, C1 -C4 -haloalkyl or C2 -C4 -haloalkenyl, and alkoxy-substituted maleic anhydrides of the formula II ##STR2## where R2 is C1 -C4 -alkyl, C2 -C4 -alkenyl, C1 -C4 -haloalkyl or C2 -C4 -haloalkenyl and Z is hydrogen, halogen or a radical OR3, where R3 is C1 -C4 -alkyl, C2 -C4 -alkenyl, C1 -C4 -haloalkyl or C2 -C4 -haloalkenyl.
The invention further relates to processes for preparing such maleimides I and the corresponding maleic anhydrides II and their use as graft monomers in graft polymers based on polyphenylene ethers.

Description

The present invention relates to novel alkoxysubstituted maleimides of the formula ##STR3## where R1 is hydrogen, C1 -C8 -alkyl, C2 -C8 -alkenyl, phenyl or phenylalkyl, and the organic radicals may furthermore carry inert substituents, and R2 and R3 are each C1 -C4 -alkyl, C2 -C4 -alkenyl, C1 -C4 -haloalkyl or C2 -C4 -haloalkenyl, and novel alkoxy-substituted maleic anhydrides of the formula II ##STR4## where R2 is C1 -C4 -alkyl, C2 -C4 -alkenyl, C1 -C4 -haloalkyl or C2 -C4 -haloalkenyl and Z is hydrogen, halogen or a radical OR3, where R3 is C1 -C4 -alkyl, C2 -C4 -alkenyl, C1 -C4 -haloalkyl or C2 -C4 -haloalkenyl.
The present invention furthermore relates to the preparation of the compounds I and II and their use as graft monomers in graft polymers based on polyphenylene ethers.
J. Heterocycl. Chem. (1972), pages 1027-1032, discloses that alkoxy-substituted maleimides can be prepared by reacting dichloromaleimides with alcoholates. However, only one halogen atom is exchanged in this reaction. An excess of alcoholate does not lead to substitution of the second halogen atom but to addition at the double bond in accordance with the following equation: ##STR5##
The second halogen atom can be exchanged only using phenolates (cf. J. Org. Chem. 37 (1972), 3637-3645). Dialkoxymaleimides and accordingly also dialkoxymaleic anhydrides are thus not obtainable in this way. Although alkoxy-substituted maleimides and maleic anhydrides are generally mentioned in various publications, for example in German Laid-Open Applications DOS 1,940,370, DOS 1,936,127 DOS 2,023,077 and DOS 3,217,658, European Pat. No. 19,296 and U.S. Pat. No. 3,816,451, no publication contains a characterization of the novel alkoxy-substituted compounds or experimental data on the alleged preparation. It must therefore be assumed that these compounds are purely speculative and have thus not been made available in practice.
It is an object of the present invention to provide the maleic acid derivatives I and II defined at the outset.
Particularly preferred radicals R1 are hydrogen and C1 -C8 -alkyl, in particular C1 -C4 -alkyl. C2 -C8 -alkenyl, phenyl and phenylalkyl are also suitable. The stated radicals may furthermore carry substituents which are inert under the reaction conditions, such as alkyl, alkoxy, haloalkyl, haloalkoxy, preferably of 1 to 4 carbon atoms, halogen, e.g. chlorine, bromine or fluorine, nitro or cyano. The following radicals may be mentioned as examples: hydrogen, methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, hexyl, heptyl, octyl, propargyl, chloroallyl, methoxymethyl, methoxyethyl, phenoxyethyl, phenyl, benzyl, phenylethyl, phenylpropyl and phenylbutyl, where the phenyl group in each case may be substituted by, for example, halogen, such as fluorine, chlorine or bromine, alkoxy, such as methoxy or ethoxy, haloalkoxy, such as fluoromethoxy, difluoromethoxy or trifluoromethoxy, alkyl, such as methyl, ethyl or propyl, or haloalkyl, such as trifluoromethyl.
Preferred radicals R2 and R3 in the compounds I and II are straight-chain or branched, unsubstituted or halogen-substituted alkyl radicals of 1 to 4 carbon atoms, e.g. methyl, ethyl, propyl, isopropyl, butyl or trifluoromethyl. Furthermore, R2 and R3 may each be C2 -C4 -alkenyl or haloalkenyl. Halogen substituents are, in particular, fluorine, chlorine or bromine.
In addition to dialkoxy-substituted maleic anhydrides II, monoalkoxy-substituted maleic anhydrides and 3-halo-4-alkoxymaleic anhydrides are also of interest, halogen being, in particular, chlorine or bromine.
We have found that this object is achieved and that the novel maleic acid derivatives can be prepared starting from a dihydroaryliminopyrrole of the formula III ##STR6## where R2 and Z have the meanings stated in claim 2 and Ar is unsubstituted or substituted aryl, as a key substance. Acidic hydrolysis of III gives the maleimides Ia, which can be converted to the N-alkyl-substituted maleimide in a conventional manner by deprotonation and reaction with an alkylating agent R1 -Y. Alkaline hydrolysis of Ia and subsequent acidic cyclization by a conventional method give the desired alkoxy-substituted maleic anhydrides II. These may in turn be converted to N-alkyl- or N-alkylphenyl-substituted maleimides by reaction with primary amines R1 NH2, or to N-phenyl-substituted maleimides by reaction with aniline or a substituted aniline. ##STR7##
According to German Laid-Open Application DOS 3,308,297, the key substance III is readily obtainable starting from pyridazinones. The aryl radical in III is, for example, phenyl or naphthyl, preferably phenyl. These radicals may carry up to 3 identical or different substituents selected from the group consisting of cyano, halogen, C1 -C4 -alkyl, C1 -C4 -alkoxy, C1 -C4 -haloalkyl and C1 -C4 -haloalkoxy. Examples of substituted aryl radicals are phenyl, α-naphthyl, β-naphthyl, fluorophenyl, difluorophenyl, chlorophenyl, dichlorophenyl, bromophenyl, dibromophenyl, trichlorophenyl, trifluoromethylphenyl, difluoromethylphenyl, methoxyphenyl, ethoxyphenyl, isopropoxyphenyl, tolyl, difluoromethoxyophenyl, trifluoromethoxyphenyl, tetrafluoroethoxyphenyl and cyanophenyl. These phenyl radicals carry the substituents in the 2-, 3-, 4-, 2,4-, 3,4-, 3,5- or 2,4,6-position.
The acidic hydrolysis of III is advantageously carried out in the presence of an aqueous acid, for example a mineral acid, such as hydrochloric acid, sulfuric acid or phosphoric acid. However, other suitable acids are strong organic acids, such as formic acid or acetic acid. The amount of acid is from 10 to 0.1, in particular from 3 to 1, moles per mole of dihydroaryliminopyrrole III. If necessary, the hydrolysis can be carried out in the presence of an organic solvent, such as low molecular weight alcohols or ethers, e.g. tetrahydrofuran, diethyl ether, methanol or ethanol.
The temperature is not particularly critical and may be from 0° to 100° C., preferably from 20° to 50° C. Depending on the reaction temperature, the hydrolysis is complete in the course of a few hours, for example from 1 to 30 hours. At temperatures below 20° C., longer reaction times are required.
The maleimides Ia are isolated in a conventional manner, for example by extraction or by filtering off the solid products and if necessary purifying them by recrystallization.
The conversion of the maleimides Ia to the N-alkyl- or N-alkenyl-substituted compounds is effected in a conventional manner by deprotonating the imides Ia by means of a base and then reacting the product with an alkylating agent. Examples of suitable bases are alkali metal hydroxides, alkaline earth metal hydroxides and alkali metal alcoholates, such as sodium hydroxide, potassium hydroxide, magnesium hydroxide, sodium methylate, potassium ethylate or sodium ethylate. The conventional compounds, such as alkyl halides, in particular chlorides, bromides or iodides, alkyl sulfates, alkyl tosylates or alkyl mesylates, can be used as the alkylating agents R1 -Y. The alkylation is carried out in a conventional manner, so that further description is unnecessary.
The preparation of the maleic anhydrides II is carried out by alkaline hydrolysis of the maleimides Ia and cyclization of the maleic acid dianion, formed as an intermediate, in the presence of an acid. If ncessary, the reaction can be carried out in the presence of a water-soluble organic solvent, for example a low molecular weight alcohol or ether. Suitable bases are alkali metal or alkaline earth metal hydroxides or carbonates, e.g. sodium hydroxide, sodium carbonate, potassium hydroxide, potassium carbonate or calcium hydroxide. The amount of base is in general from 1 to 3 equivalents, based on maleimide Ia.
The hydrolysis can be carried out at from 0° to 100° C., in particular from 20° to 50° C. When the hydrolysis is complete, the reaction mixture is acidified and the anhydride formed can be isolated in a conventional manner, for example by extraction or by separating it off by filtration.
The conversion of the anhydrides II into maleimides can be carried out in a conventional manner by reacting the anhydrides II with primary amines R1 NH2, where R1 has the meanings stated in claim 1. The reaction can be carried out, for example, as described in German Laid-Open Application DOS 3,222,152, so that further description is unnecessary.
We have found that the novel maleimides I and maleic anhydrides II can be used as monomer components is polymeric systems, in particular as graft monomers in graft polymers based on polyphenylene ethers, with the result that particularly good melt flow in combination with little intrinsic color of the graft polymer is obtained. The graft polymers can be prepared in principle as described in the German Laid-Open Application 3,540,119 or 3,621,207 or in contemporaneous application 37 15 343.9.
Furthermore, the novel compounds I and II can be used as intermediates in organic syntheses, for example for the preparation of dyes, drugs or crop protection agents.
EXAMPLE 1 Preparation of dimethoxymaleimide
500 g of 2,5-dihydro-3,4-dimethoxy-5-phenyliminopyrrol-2-one were stirred with 500 ml of concentrated hydrochloric acid in 2 l of water for 2 days at room temperature. Thereafter, the mixture was cooled and filtered under suction. 325 g of dimethoxymaleimide of melting point 126°-127° C. were obtained.
EXAMPLE 2 Preparation of dimethoxymaleic anhydride
555 g of dimethoxymaleimide in 2 l of 5% strength NaOH were stirred for 2 days at room temperature. Thereafter, the mixture was acidified and extracted thoroughly with methylene chloride. After the organic phase had been separated off and the solvent removed in a rotary evaporator, 486 g of a product of melting point 41°-43° C. remained.
EXAMPLE 3
99 kg of poly-(2,6-dimethyl-1,4-phenylene)ether having a relative viscosity of 0.50, measured in 1% strength by weight chloroform solution at 25° C., and 1 kg of monomer Z were reacted with one another in a twinscrew extruder of the type ZKS 53 (Werner and Pfleiderer) at 270° C. and then devolatilized in a devolatilization zone at 280° C. under reduced pressure. The mean residence time in the extruder was 3.5 minutes. The melt was cooled by passing it through a water bath, and was granulated and dried. The granules were soluble in toluene. The results are summarized in the Table below:
______________________________________                                    
Monomer Z         Relative viscosity                                      
                               Color                                      
______________________________________                                    
Dimethoxymaleic anhydride                                                 
                  0.55         pale                                       
Dimethoxymaleimide                                                        
                  0.57         pale                                       
3-Chloro-4-methoxymaleic                                                  
                  0.53         pale                                       
anhydride                                                                 
Comparison                                                                
2-Ethylhexyl monomaleate                                                  
                  0.64         pale                                       
No monomer        0.53         pale                                       
Maleic anhydride  0.73         dark                                       
______________________________________
Comparison with prior art monomers shows the slight increase in viscosity when novel graft monomers are used.

Claims (2)

We claim:
1. A process for the preparation of a maleic anhydride ##STR8## where R2 is C1 -C4 -alkyl, C2 -C4 -alkenyl, C1 -C4 -haloalkyl or C2 -C4 -haloalkenyl and Z is hydrogen, halogen or a radical OR3, where R3 is C1 -C4 -alkyl, C2 -C4 -alkenyl, C1 -C4 -haloalkyl or C2 -C4 -haloalkenyl, which comprises:
subjecting a maleimide ##STR9## to alkaline hydrolysis at 0° to 100° C. and cyclizing the resulting maleic acid dianion in the presence of an acid to give the anhydride II; and
isolating said anhydride II which has been formed in the reaction mixture.
2. A process as claimed in claim 1 wherein the hydrolysis is carried out at a temperature of about 20° to 50° C.
US07/592,847 1987-05-08 1990-10-04 Preparation of alkoxy maleic anhydrides Expired - Lifetime USRE33820E (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19873715344 DE3715344A1 (en) 1987-05-08 1987-05-08 ALKOXY-SUBSTITUTED MALEINIC ACID IMIDES AND MALEIC ACID ANHYDRIDES, METHODS FOR THEIR PRODUCTION AND THEIR USE
DE3715344 1987-05-08

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US07/189,297 Reissue US4877887A (en) 1987-05-08 1988-05-02 Preparation of alkoxy maleic anhydrides

Publications (1)

Publication Number Publication Date
USRE33820E true USRE33820E (en) 1992-02-11

Family

ID=6327097

Family Applications (2)

Application Number Title Priority Date Filing Date
US07/189,297 Ceased US4877887A (en) 1987-05-08 1988-05-02 Preparation of alkoxy maleic anhydrides
US07/592,847 Expired - Lifetime USRE33820E (en) 1987-05-08 1990-10-04 Preparation of alkoxy maleic anhydrides

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US07/189,297 Ceased US4877887A (en) 1987-05-08 1988-05-02 Preparation of alkoxy maleic anhydrides

Country Status (4)

Country Link
US (2) US4877887A (en)
EP (1) EP0289925B1 (en)
JP (1) JPS63297362A (en)
DE (2) DE3715344A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3822121A1 (en) * 1988-06-30 1990-03-01 Hoechst Ag CHIRAL SUBSTITUTED TARTIC ACID IMIDES, METHOD FOR THE PRODUCTION THEREOF AND THE USE THEREOF AS A DOPE IN LIQUID CRYSTAL MIXTURES
US5364945A (en) * 1994-01-03 1994-11-15 The Sherwin-Williams Company Anhydride-functional monomers and polymers and reactive compositions prepared from same
CN103483327A (en) * 2013-09-03 2014-01-01 福建师范大学 Method for preparing multiple-stimulation respond material containing thienylmaleimide by virtue of dehydration reaction process

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE193612C (en) *
DE202307C (en) *
DE321765C (en) * 1912-07-31 1920-06-14 Pierre Joseph Grandsire Fils Device for bleaching and dyeing coetzers
GB1280747A (en) * 1969-07-16 1972-07-05 Bayer Ag New carboxylic acid imide derivatives
US3816451A (en) * 1971-11-02 1974-06-11 Abbott Lab Maleimide derivatives as plant growth regulators
EP0019296A1 (en) * 1979-05-21 1980-11-26 Union Carbide Corporation Process for removing triorganophosphine from a liquid composition
US4417028A (en) * 1981-05-11 1983-11-22 Loctite Corporation Preapplied plastic film adhesive composition
DE3222152A1 (en) * 1982-06-12 1983-12-15 Bayer Ag, 5090 Leverkusen SUBSTITUTED MALEINIC ACID IMIDES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A PEST CONTROL

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1936127A1 (en) * 1969-07-16 1971-01-28 Bayer Ag New Carboximide Derivatives
DE1940370A1 (en) * 1969-07-16 1971-02-18 Bayer Ag New Dicarboximides

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE193612C (en) *
DE202307C (en) *
DE321765C (en) * 1912-07-31 1920-06-14 Pierre Joseph Grandsire Fils Device for bleaching and dyeing coetzers
GB1280747A (en) * 1969-07-16 1972-07-05 Bayer Ag New carboxylic acid imide derivatives
US3816451A (en) * 1971-11-02 1974-06-11 Abbott Lab Maleimide derivatives as plant growth regulators
EP0019296A1 (en) * 1979-05-21 1980-11-26 Union Carbide Corporation Process for removing triorganophosphine from a liquid composition
US4417028A (en) * 1981-05-11 1983-11-22 Loctite Corporation Preapplied plastic film adhesive composition
DE3222152A1 (en) * 1982-06-12 1983-12-15 Bayer Ag, 5090 Leverkusen SUBSTITUTED MALEINIC ACID IMIDES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A PEST CONTROL
US4582849A (en) * 1982-06-12 1986-04-15 Bayer Aktiengesellschaft Fungicidal N-substituted maleic acid imides

Non-Patent Citations (16)

* Cited by examiner, † Cited by third party
Title
Clemo et al., J. Chem. Soc. Perkin I, pp. 1448 1453 (1981). *
Clemo et al., J. Chem. Soc. Perkin I, pp. 1448-1453 (1981).
Cope, J.A.C.S., 58, pp. 570 572 (1936). *
Cope, J.A.C.S., 58, pp. 570-572 (1936).
Khan, J. of Pharmaceutical Sciences, 73 (12), pp. 1767 1771 (1984). *
Khan, J. of Pharmaceutical Sciences, 73 (12), pp. 1767-1771 (1984).
Lynch et al., J. of Heterocyclic Chemistry, Oct. 1972, pp. 1027 1032. *
Lynch et al., J. of Heterocyclic Chemistry, Oct. 1972, pp. 1027-1032.
Relles et al., Journal of Organic Chemistry, 37, 3637 45 (1972). *
Relles et al., Journal of Organic Chemistry, 37, 3637-45 (1972).
Rothhaas, Annalen. der Chemie, 501, pp. 295 304 (1933). *
Rothhaas, Annalen. der Chemie, 501, pp. 295-304 (1933).
Schmidt et al., Chem. Ber., 115, pp. 2674 2678 (1982). *
Schmidt et al., Chem. Ber., 115, pp. 2674-2678 (1982).
Yeh et al., Tet. Letters, No. 42, pp. 3987 3988 (1978). *
Yeh et al., Tet. Letters, No. 42, pp. 3987-3988 (1978).

Also Published As

Publication number Publication date
EP0289925A3 (en) 1989-08-30
DE3861814D1 (en) 1991-04-04
EP0289925B1 (en) 1991-02-27
EP0289925A2 (en) 1988-11-09
DE3715344A1 (en) 1988-11-24
US4877887A (en) 1989-10-31
JPS63297362A (en) 1988-12-05

Similar Documents

Publication Publication Date Title
US5708175A (en) Process for producing 4-trifluoromethylnicotinic acid
US4492796A (en) Isoindolenine derivatives, processes for their preparation and their use as intermediate products for the preparation of dyestuffs
US4824949A (en) Process for the preparation of pyrimidines
USRE33820E (en) Preparation of alkoxy maleic anhydrides
US5229521A (en) Process for the preparation of symmetrical 2,2-methylenebisbenzotriazolyl phenols
KR100720220B1 (en) Process for producing substituted aniline compound
EP0634409A1 (en) Process of producing 2-cyano-4-oxo-4H-benzopyran compounds
US4895950A (en) 5-halogeno-6-amino-nicotinic acid halides
Médebielle et al. Tetrakis (dimethylamino) ethylene (TDAE) mediated addition of heterocyclic difluoromethyl anions to heteroaryl aldehydes. A facile synthetic method for new gem-difluorinated alcohols derived from 4-bromo-1-naphthylamine and 8-quinolylamine
US5696272A (en) Process for the production of 2-substituted 5-chloroimidazole-4-carbaldehydes
US4965363A (en) Process for the preparation of 3-cyano-4-aryl-pyrroles
US4213905A (en) Preparation of 5-aroyl-1-loweralkylpyrrole-2-acetic acid salts
US5066825A (en) Process for preparing a naphthalene derivative
JP3159405B2 (en) Method for producing thienyl ether derivative
US4450308A (en) Process for the preparation of trifluoromethylphenyl oxyphenyl ether compounds
US4112003A (en) Process for preparing polyphenols
EP0574952A1 (en) Process for preparing 2-oxopyrrolidinylacetamide derivatives
CA2117034C (en) Process for the production of 2-substituted-5-chlorimidazole-4-carbaldehydes
Ohba et al. Synthesis of Ethenylbenzothiazole Derivatives
US5659064A (en) Hydrazone intermediates
US4383116A (en) Process for producing 4-benzoylpyrazoles
KR880001850B1 (en) Preparation process for derivertives of 5-fluoro pyridone
US4923993A (en) Process for the preparation of 2-pyridinecarboxylic acid derivatives and 1-amino-1,4-dihydropyridine-2-carboxylic acid derivatives
US5633380A (en) Substituted quinoline herbicide intermediates and process
JP3388046B2 (en) Method for producing thienyl ether derivative

Legal Events

Date Code Title Description
FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

FPAY Fee payment

Year of fee payment: 12