JPS6425743A - Production of trans-chrysanthemum-monocarboxylic acids - Google Patents
Production of trans-chrysanthemum-monocarboxylic acidsInfo
- Publication number
- JPS6425743A JPS6425743A JP62164803A JP16480387A JPS6425743A JP S6425743 A JPS6425743 A JP S6425743A JP 62164803 A JP62164803 A JP 62164803A JP 16480387 A JP16480387 A JP 16480387A JP S6425743 A JPS6425743 A JP S6425743A
- Authority
- JP
- Japan
- Prior art keywords
- trans
- chrysanthemum
- hydrogen bromide
- cis
- bromide
- 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
Landscapes
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
PURPOSE:To obtain the titled compound useful as a raw material for insecticide for pyrethroid type smoothly and efficiently, by treating a trans-chrysanthemum- monocarboxylic acid of a mixture of trans-form and cis-form with hydrogen bromide which is common as an industrial raw material, stable to water and readily handleable. CONSTITUTION:A trans-chrysanthemum-monocarboxylic acid (R is H, 1-20C alkyl, cycloalkyl or aralkyl) of cis-form or a mixture of trans-form and cis-form is treated with hydrogen bromide in the presence or absence of a peroxide or an azo compound usually at -20-100 deg.C and made into trans-form to give the aimed compound. Hydrogen bromide may be in a gaseous state, in a dissolved state in a solvent or in an emitted state in the reaction system by using both a bromide such as lithium bromide and an acid such as sulfuric acid. The amount of hydrogen bromide used is usually 1/1,000-1/4mol. based on 1mol. chrysanthemum-monocarboxylic acid used.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62164803A JPH0717566B2 (en) | 1987-04-07 | 1987-06-30 | Method for producing racemic-trans primary chrysanthemic acids |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62-86595 | 1987-04-07 | ||
JP8659587 | 1987-04-07 | ||
JP62164803A JPH0717566B2 (en) | 1987-04-07 | 1987-06-30 | Method for producing racemic-trans primary chrysanthemic acids |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6425743A true JPS6425743A (en) | 1989-01-27 |
JPH0717566B2 JPH0717566B2 (en) | 1995-03-01 |
Family
ID=26427706
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62164803A Expired - Fee Related JPH0717566B2 (en) | 1987-04-07 | 1987-06-30 | Method for producing racemic-trans primary chrysanthemic acids |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0717566B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS646234A (en) * | 1986-09-04 | 1989-01-10 | Sumitomo Chemical Co | Racemization of optically active chrysanthemum-monocarboxylic acids |
JPH0327343A (en) * | 1989-06-23 | 1991-02-05 | Sumitomo Chem Co Ltd | Production of trans-chrysanthemumic acids |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS646234A (en) * | 1986-09-04 | 1989-01-10 | Sumitomo Chemical Co | Racemization of optically active chrysanthemum-monocarboxylic acids |
-
1987
- 1987-06-30 JP JP62164803A patent/JPH0717566B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS646234A (en) * | 1986-09-04 | 1989-01-10 | Sumitomo Chemical Co | Racemization of optically active chrysanthemum-monocarboxylic acids |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS646234A (en) * | 1986-09-04 | 1989-01-10 | Sumitomo Chemical Co | Racemization of optically active chrysanthemum-monocarboxylic acids |
JPH0327343A (en) * | 1989-06-23 | 1991-02-05 | Sumitomo Chem Co Ltd | Production of trans-chrysanthemumic acids |
Also Published As
Publication number | Publication date |
---|---|
JPH0717566B2 (en) | 1995-03-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
S531 | Written request for registration of change of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313531 |
|
S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
R370 | Written measure of declining of transfer procedure |
Free format text: JAPANESE INTERMEDIATE CODE: R370 |
|
S531 | Written request for registration of change of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313531 |
|
S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
LAPS | Cancellation because of no payment of annual fees |