JPS5636434A - Preparation of tartaric acid or epoxysuccinic acid diester - Google Patents
Preparation of tartaric acid or epoxysuccinic acid diesterInfo
- Publication number
- JPS5636434A JPS5636434A JP11104479A JP11104479A JPS5636434A JP S5636434 A JPS5636434 A JP S5636434A JP 11104479 A JP11104479 A JP 11104479A JP 11104479 A JP11104479 A JP 11104479A JP S5636434 A JPS5636434 A JP S5636434A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- epoxysuccinic
- catalyst
- tartaric
- tartaric acid
- 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.)
- Granted
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Abstract
PURPOSE: To prepare the titled compound useful as a raw material of resins, etc., easily, suppressing the side reactions, by reacting tartaric acid or epoxysuccinic acid with an unsaturated alcohol in the presence of an organic sulfonic acid compound as a catalyst.
CONSTITUTION: The titled compound is prepared by reacting (A) (1mol of) tartaric acid or epoxysuccinic acid with (B) pref. 2W300mol, especially 5W200mol of) an unsaturated alcohol such as allyl alcohol, methallyl alcohol, etc., in the presence of (C) a catalyst comprising an organic sulfonic acid e.g. aliphatic hydrocarbon sulfonic acid such as ethanesulfonic acid or an aromatic hydrocarbon sulfonic acid such as naphthalenesulfonic acid. The amount of the catalyst is 0.0001W 1mol, pref. 0.001W0.5mol/mol of tartaric acid or epoxysuccinic acid.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11104479A JPS5636434A (en) | 1979-09-01 | 1979-09-01 | Preparation of tartaric acid or epoxysuccinic acid diester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11104479A JPS5636434A (en) | 1979-09-01 | 1979-09-01 | Preparation of tartaric acid or epoxysuccinic acid diester |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5636434A true JPS5636434A (en) | 1981-04-09 |
JPS6310692B2 JPS6310692B2 (en) | 1988-03-08 |
Family
ID=14550982
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11104479A Granted JPS5636434A (en) | 1979-09-01 | 1979-09-01 | Preparation of tartaric acid or epoxysuccinic acid diester |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5636434A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6163637A (en) * | 1984-09-03 | 1986-04-01 | Toray Ind Inc | Production of lactic acid ester |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0521592U (en) * | 1991-08-30 | 1993-03-19 | 松下電器産業株式会社 | Code clip for remote control |
-
1979
- 1979-09-01 JP JP11104479A patent/JPS5636434A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6163637A (en) * | 1984-09-03 | 1986-04-01 | Toray Ind Inc | Production of lactic acid ester |
JPH0577662B2 (en) * | 1984-09-03 | 1993-10-27 | Toray Industries |
Also Published As
Publication number | Publication date |
---|---|
JPS6310692B2 (en) | 1988-03-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS5636434A (en) | Preparation of tartaric acid or epoxysuccinic acid diester | |
JPS5452043A (en) | Preparation of peroxide | |
JPS5291810A (en) | Preparation of alkylene glycols | |
JPS56152457A (en) | Preparation of peroxide | |
JPS53141216A (en) | Preparation of methacrylic acid ester | |
JPS5410399A (en) | Preparation of polyalkylene glycol derivative | |
JPS57118527A (en) | Preparation of ethylene glycol | |
JPS5639032A (en) | Preparation of hydroxyhydrocarbon ethers | |
JPS5325504A (en) | Isolation of glycols | |
IE792291L (en) | Process for the manufacture of 5-mercapto-1,2,3-triazoles. | |
JPS5414909A (en) | Preparation of ethers | |
JPS56113745A (en) | Preparation of bromonitroalcohol | |
JPS5430104A (en) | Continuous production of tertiary butyl alcohol | |
JPS5683486A (en) | Preparation of 1,3-benzodioxol-5-ol | |
JPS5262232A (en) | Alkoxylation process for halogenated diphenyls | |
JPS5564551A (en) | Preparation of dialkyl carbonate | |
JPS57209639A (en) | Preparation of silver catalyst | |
JPS5515427A (en) | Preparation of olefin oxide | |
JPS51138650A (en) | Process for preparing optically active trans-cyclopentene-3,5,-diolmon oester | |
JPS5291838A (en) | Preparation of oxybenzoic acid diesters | |
JPS5579334A (en) | Preparation of methylphenol | |
JPS5731629A (en) | Preparation of bisphenolethane | |
JPS5427507A (en) | Preparation of tertiary butyl alcohol | |
JPS55133371A (en) | Preparation of gamma-alkyl-gamma-lactone | |
JPS56166141A (en) | Preparation of phenoxybenzaldehyde |