JPS56135440A - Preparation of m-phenoxybenzaldehyde - Google Patents
Preparation of m-phenoxybenzaldehydeInfo
- Publication number
- JPS56135440A JPS56135440A JP3788280A JP3788280A JPS56135440A JP S56135440 A JPS56135440 A JP S56135440A JP 3788280 A JP3788280 A JP 3788280A JP 3788280 A JP3788280 A JP 3788280A JP S56135440 A JPS56135440 A JP S56135440A
- Authority
- JP
- Japan
- Prior art keywords
- fatty acid
- lower fatty
- chloride
- mixture
- 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.)
- 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
Abstract
PURPOSE: To obtain the titled compound useful as an intermediate for an insecticide in high yield at a high reaction rate, by esterifying benzal inexpensive m-phenoxybensyl chloride in its mixture with chloride as raw materials with a lower fatty acid, and oxidizing the ester with nitric acid, in the presence of a specific surfactant.
CONSTITUTION: A mixture of m-phenoxybenzyl chloride with m-phenoxybenzal chloride as raw materials is reacted with a lower fatty acid and an alkali metallic salt of a lower fatty acid in the presence of water in an amount of 20wt% or less based on the lower fatty acid, at 100W200°C, to prepare a mixture of a lower fatty acid ester of m-phenoxybenzyl alcohol with m-phenoxybenzaldehyde. The resultant mixture is then reacted with 1W10wt% dilute nitric acid in the presence of an anionic surfactant of a sulfonic acid type, to give the aimed compound.
EFFECT: The secondary oxidation into m-phenoxybenzoic acid is suppressed.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3788280A JPS56135440A (en) | 1980-03-25 | 1980-03-25 | Preparation of m-phenoxybenzaldehyde |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3788280A JPS56135440A (en) | 1980-03-25 | 1980-03-25 | Preparation of m-phenoxybenzaldehyde |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS56135440A true JPS56135440A (en) | 1981-10-22 |
Family
ID=12509902
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3788280A Pending JPS56135440A (en) | 1980-03-25 | 1980-03-25 | Preparation of m-phenoxybenzaldehyde |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56135440A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103274929A (en) * | 2013-04-09 | 2013-09-04 | 金凯(辽宁)化工有限公司 | Preparation method of 2-trifluoromethyl benzoic acid |
-
1980
- 1980-03-25 JP JP3788280A patent/JPS56135440A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103274929A (en) * | 2013-04-09 | 2013-09-04 | 金凯(辽宁)化工有限公司 | Preparation method of 2-trifluoromethyl benzoic acid |
CN103274929B (en) * | 2013-04-09 | 2014-12-17 | 金凯(辽宁)化工有限公司 | Preparation method of 2-trifluoromethyl benzoic acid |
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