JPS57175143A - Preparation of o-or m-chlorobenzoic acid - Google Patents
Preparation of o-or m-chlorobenzoic acidInfo
- Publication number
- JPS57175143A JPS57175143A JP56059783A JP5978381A JPS57175143A JP S57175143 A JPS57175143 A JP S57175143A JP 56059783 A JP56059783 A JP 56059783A JP 5978381 A JP5978381 A JP 5978381A JP S57175143 A JPS57175143 A JP S57175143A
- Authority
- JP
- Japan
- Prior art keywords
- chlorotoluene
- metal
- compound
- chlorobenzoic acid
- expressed
- 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 obtain the titled compound at a high reaction rate in a high conversion with the inhibited formation of a tarry substance as a by-product, by oxidizing chlorotoluene with a gas containing molecular oxygen in the presence of a reaction product and a catalyst containing Co, Mn and Br without using a solvent.
CONSTITUTION: o-or m-Chlorotoluene is oxidixed with a gas containing molecular oxygen to prepare the corresponding chlorobenzoic acid. In the process, a catalytic system containing Co, Mn and Br essentially is used, and chlorobenzoic acid which is the aimed product in an amount of 20wt% or more based on the raw material chlorotoluene is present in the reaction system to carry out the reaction at 120W200°C, preferably 130W180°C. Preferably the amounts of the Co, Mn and Br are as follows: 0.02W0.7wt%, expressed in terms of Co metal, based on the chlorotoluene, Co compound, 2W20wt%, expressed in terms of Mn metal, based on the Co metal, Mn compound and a Br compound in an amount of 2W5 times that of Co metal expressed in terms of Br atom.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56059783A JPS57175143A (en) | 1981-04-22 | 1981-04-22 | Preparation of o-or m-chlorobenzoic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56059783A JPS57175143A (en) | 1981-04-22 | 1981-04-22 | Preparation of o-or m-chlorobenzoic acid |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57175143A true JPS57175143A (en) | 1982-10-28 |
JPS6412258B2 JPS6412258B2 (en) | 1989-02-28 |
Family
ID=13123228
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56059783A Granted JPS57175143A (en) | 1981-04-22 | 1981-04-22 | Preparation of o-or m-chlorobenzoic acid |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57175143A (en) |
-
1981
- 1981-04-22 JP JP56059783A patent/JPS57175143A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6412258B2 (en) | 1989-02-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS5323939A (en) | Preparation of divalent phenols | |
JPS5223589A (en) | Catalyst for producing alpha,beta-unsaturaded carboxylic acid | |
JPS57175143A (en) | Preparation of o-or m-chlorobenzoic acid | |
JPS54151932A (en) | Preparation of ubiquinone | |
JPS57123811A (en) | Production of carbon monoxide | |
JPS532436A (en) | Preparation of phenols | |
JPS5210248A (en) | Process for preparation of alpha-tetralone | |
JPS5253805A (en) | Preparation of hexafluoropropylene epoxide | |
JPS52133942A (en) | Treatment of reaction mother liquor | |
JPS55133321A (en) | Preparation of perfluoro-2-butene | |
JPS5444605A (en) | Preparation of methanol | |
JPS56158720A (en) | Production of oxygen compound | |
JPS54163509A (en) | Preparation of methacrolein | |
JPS57114583A (en) | Preparation of 2,3-epoxycyclohexan-1-ol | |
JPS53103414A (en) | Preparation of acrylic acid | |
JPS5359639A (en) | Preparation of terephthalic acid | |
JPS5692832A (en) | Preparation of aromatic polycarboxylic acid | |
JPS5731629A (en) | Preparation of bisphenolethane | |
JPS525718A (en) | Process for preparation of divalent phenols | |
JPS5592338A (en) | Preparation of methyl ethyl ketone | |
JPS57181040A (en) | Preparation of m-nitrobenzoic acid | |
JPS57181034A (en) | Preparation of p-chlorobenzoic acid | |
JPS56156240A (en) | Preparation of 1-dimethylamino-3-methyl-2-butene | |
JPS5657720A (en) | Preparation of 1,1,2-trichloroethane and ammonia | |
JPS52100415A (en) | Production of trimethylolacetic acid |