JPS57142940A - Preparation of suberic acid - Google Patents
Preparation of suberic acidInfo
- Publication number
- JPS57142940A JPS57142940A JP56027630A JP2763081A JPS57142940A JP S57142940 A JPS57142940 A JP S57142940A JP 56027630 A JP56027630 A JP 56027630A JP 2763081 A JP2763081 A JP 2763081A JP S57142940 A JPS57142940 A JP S57142940A
- Authority
- JP
- Japan
- Prior art keywords
- cyclooctene
- raw material
- hydrogen peroxide
- propionic acid
- amount
- 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.)
- Pending
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
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PURPOSE: To obtain suberic acid which is a raw material for resins and an intermediate for agricultural chemicals in high purity and yield without forming reaction by-products, by reacting cyclooctene with ozone in propionic acid solvent, and oxidizing the reaction product withe hydrogen peroxide containing a specific oxyacid.
CONSTITUTION: The ozonolysis of cyclooctene is carried out by reacting the cyclooctene with oxygen containing ozone or air in propionic acid solvent at +20W-20°C, preferably, -10W-20°C, and the ozonolysis products is reacted with hydrogen peroxide in presence of an oxyacid, having the maximal oxidation number, and obtained from a nonmetallic element of Group VB or VIB in the periodic table in a catalytic amount, e.g. sulfuric acid or p-toluenesulfonic acid, at 60W80°C and oxidized at the refluxing temperature of the propionic acid solvent to give the aimed compound. The amount of the hydrogen peroxide is preferably equimolar with the raw material cyclooctene or a slight excess, and the amount of the acidic catalyst is 1W20mol% based on the raw material.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56027630A JPS57142940A (en) | 1981-02-28 | 1981-02-28 | Preparation of suberic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56027630A JPS57142940A (en) | 1981-02-28 | 1981-02-28 | Preparation of suberic acid |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS57142940A true JPS57142940A (en) | 1982-09-03 |
Family
ID=12226269
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56027630A Pending JPS57142940A (en) | 1981-02-28 | 1981-02-28 | Preparation of suberic acid |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57142940A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012201685A (en) * | 2011-03-25 | 2012-10-22 | Evonik Degussa Gmbh | SYNTHESIS OF α,ω-DICARBOXYLIC ACID AND ESTER THEREOF FROM UNSATURATED FATTY ACID DERIVATIVE |
-
1981
- 1981-02-28 JP JP56027630A patent/JPS57142940A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012201685A (en) * | 2011-03-25 | 2012-10-22 | Evonik Degussa Gmbh | SYNTHESIS OF α,ω-DICARBOXYLIC ACID AND ESTER THEREOF FROM UNSATURATED FATTY ACID DERIVATIVE |
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