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Method for production of maleimides

Assignee: Nippon Shokubai Co Ltd
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Filing: 1986-10-27
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Granted: 1988-11-22
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Expires: 2006-10-27
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Abstract

Abstract A method for the production of maleimides, which comprises subjecting maleinamic acids to ring-closure imidation in an organic solvent capable of forming an azeotrope with water in the presence of an acid catalyst at a temperature in the range of 120° to 250° C. while removing the formed water in the form of an azeotrope with said organic solvent and thereafter purifying the produced maleimides.

Inventors

  • 👤 Yuichi Kita
  • 👤 Kentaro Sakamoto
  • 👤 Masao Baba
  • 👤 Atsushi Okubo

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 17:50
CPC Classifications
C; C07; C07D; C07D207/00; C07D207/02; C07D207/44; C07D207/444; C07D207/448

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 200 words
A method for the production of maleimides, which comprises subjecting maleinamic acids to ring-closure imidation in an organic solvent capable of forming an azeotrope with water in the presence of an acid catalyst at a temperature in the range of 120° to 250° C. while removing the formed water in the form of an azeotrope with said organic solvent and thereafter purifying the produced maleimides, wherein said purification comprises adding to crude maleimides an organic acid or inorganic acid selected from the group consisting of ortho-phosphoric acid, pyrophosphoric acid, sulfuric acid, sulfuric acid anhydride, fuming sulfuric scid, methane sulfonic acid, chlorosulfonic acid, chloromaleic acid, para-toluenesulfonic acid and trifluoroacetic acid in an amount of from about 5 to about 30% by weight based on the maleinamic acids used as the raw material, heating the resultant mixture at a temperature in the range of 20° to 100° C., removing the resinous impurities formed, separating the organic product containing phase from the aqueous acid phase and washing the resultant organic layer with a sufficient amount of water to remove the water-soluble impurities from the organic layer and removing the solvent portion of the organic phase under reduced pressure to yield essentially pure maleimide.
Claim 2
Independent Claim 200 words
A method for the production of maleimides, which comprises subjecting maleinamic acids to ring-closure imidation in an organic solvent capable of forming an azeotrope with water in the presence of an acid catalyst at a temperature in the range of 120° to 250° C. while removing the formed water in the form of an azeotrope with said organic solvent and thereafter purifying the produced maleimides, wherein said purification comprises adding to crude maleimides an organic acid or inorganic acid selected from the group consisting of ortho-phosphoric acid, pyrophosphoric acid, sulfuric acid, sulfuric acid anhydride, fuming sulfuric scid, methane sulfonic acid, chlorosulfonic acid, chloromaleic acid, para-toluenesulfonic acid and trifluoroacetic acid in an amount of from about 5 to about 30% by weight based on the maleinamic acids used as the raw material, heating the resultant mixture at a temperature in the range of 20° to 100° C., removing the resinous impurities formed, separating the organic product containing phase from the aqueous acid phase and washing the resultant organic layer with a sufficient amount of water to remove the water-soluble impurities from the organic layer and removing the solvent portion of the organic phase under reduced pressure to yield essentially pure maleimide.
Claim 3
Dependent Claim 29 words
A method according to claim 1 wherein said acid is at least one acid selected from the group consisting of sulfuric acid, sulfuric acid anhydride and fuming sulfuric acid.
Claim 4
Dependent Claim 26 words
A method according to claim 1 wherein said washing with water is carried out using 1 to 5 times of water to said starting maleinamic acids.

References Cited (Backward Citations)

DE2100800A1 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-11-22 1992-05-23 1992-11-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-11-22 1996-05-23 1996-11-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-11-22 2000-05-23 2000-11-22 $7700.00 Window Closed / Lapsed

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