JPS5767543A - Preparation of 2-amino-4,6-dichloro-5-methylphenol - Google Patents
Preparation of 2-amino-4,6-dichloro-5-methylphenolInfo
- Publication number
- JPS5767543A JPS5767543A JP55144034A JP14403480A JPS5767543A JP S5767543 A JPS5767543 A JP S5767543A JP 55144034 A JP55144034 A JP 55144034A JP 14403480 A JP14403480 A JP 14403480A JP S5767543 A JPS5767543 A JP S5767543A
- Authority
- JP
- Japan
- Prior art keywords
- dichloro
- titled compound
- pressure
- nitro
- phenol
- 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
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
PURPOSE: To obtain the titled compound which is an intermediate for a photographic chemical safely and easily in high purity and yield, by reducing 2-nitro-4, 6- dichloro-5-methyl-phenol in an aqueous solution of a caustic alkali in the presence of a catalyst under specific conditions.
CONSTITUTION: 2-Nitro-4,6-dichloro-5-methyl-phenol in an aqueous solution of a caustic alkali in an equivalent amount or more is reacted with hydrogen in the resence of a Rney nickel catalyst to give the titled compound. The reaction is carried out at a pressure ≤3kg/cm2 (gauge pressure), preferably ordinary pressure, and 40°C or below. The operation is carried out easily and safely due to the absence of organic solvents. The titled compound of high grade can be obtained almost quantitatively without forming by-products.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55144034A JPS5767543A (en) | 1980-10-14 | 1980-10-14 | Preparation of 2-amino-4,6-dichloro-5-methylphenol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55144034A JPS5767543A (en) | 1980-10-14 | 1980-10-14 | Preparation of 2-amino-4,6-dichloro-5-methylphenol |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5767543A true JPS5767543A (en) | 1982-04-24 |
Family
ID=15352778
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP55144034A Pending JPS5767543A (en) | 1980-10-14 | 1980-10-14 | Preparation of 2-amino-4,6-dichloro-5-methylphenol |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5767543A (en) |
-
1980
- 1980-10-14 JP JP55144034A patent/JPS5767543A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS57116038A (en) | Preparation of 3-cyano-3,5,5-trimethylcyclohexanone | |
JPS5767543A (en) | Preparation of 2-amino-4,6-dichloro-5-methylphenol | |
JPS55149294A (en) | Preparation of triphenylphosphine | |
JPS55129257A (en) | Purification of acetonitrile containing hydrogen cyanide | |
JPS5581818A (en) | Method of fluorination | |
JPS5492968A (en) | Preparation of 2-pentynyl ether | |
JPS5487754A (en) | Production of hydroxypropylcellulose | |
JPS5699448A (en) | Preparation of lower alkoxyaniline | |
JPS5675462A (en) | Preparation of benzenecarboxylate | |
JPS5373529A (en) | Preparation of hydroquinone | |
JPS5686146A (en) | Preparation of lower aliphatic isocyanate | |
JPS57169447A (en) | Preparation of 2,4-dichloro- or 2,6-dichloroaniline | |
JPS56167633A (en) | Preparation of carbonyl compound | |
JPS5430104A (en) | Continuous production of tertiary butyl alcohol | |
JPS52122330A (en) | Preparation of 2-(o-nitrophenyl)ethanols | |
JPS5325504A (en) | Isolation of glycols | |
JPS56154442A (en) | Recovery of 2,2'-dimethyl-4-hydroxydiphenylamine, on production of 4-amino-3-methylphenol | |
JPS54130526A (en) | Preparation of o-chloroaniline | |
JPS57179154A (en) | Preparation of 2,2'-dihydroxy-1,1'-dinaphthyl disulfide | |
JPS5590501A (en) | Preparation of ethylcarboxymethylcellulose | |
JPS572243A (en) | Preparation of nitrodiphenylamine | |
JPS5697239A (en) | Recovering method of isooctyl alcohol | |
JPS57142948A (en) | Preparation of cyclopentylamine | |
JPS53105471A (en) | Preparation of cyclic ethers | |
JPS5731668A (en) | Preparation of 4,5-dicarbamoylimidazole |