JPS5683430A - Preparation of pyrogallol - Google Patents
Preparation of pyrogallolInfo
- Publication number
- JPS5683430A JPS5683430A JP16109779A JP16109779A JPS5683430A JP S5683430 A JPS5683430 A JP S5683430A JP 16109779 A JP16109779 A JP 16109779A JP 16109779 A JP16109779 A JP 16109779A JP S5683430 A JPS5683430 A JP S5683430A
- Authority
- JP
- Japan
- Prior art keywords
- cyclohexanetriol
- pref
- pyrogallol
- catalyst
- group metal
- 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
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PURPOSE: To prepare pyrogallol useful as an intermediate for the organic syntheses of bioactive substances, etc., in high selectivity, by the dehydrogenation of 1,2,3- cyclohexanetriol in an inert gas stream in the presence of a Pt-group metal catalyst.
CONSTITUTION: Pyrogallol is prepared by the dehydrogenation of 1,2,3-cyclohexanetriol in the presence of a catalyst comprising a Pt-group metal such as Ir, Rh, Pd, etc. or a Pt-group metal added with an alkali metal compound such as K2CO3, and pref. supported on a carrier such as activated charcoal, in an inert gas stream which does not participate in the reactions, e.g. N2 and CO2, at 150W350°C under atmospheric or reduced pressure. The reaction is pref. carried out in the vapor phase to prevent the dissolution of the alkali metal compound. 1,2,3-Cyclohexanetriol is pref. used as an aqueous solution because the presence of water in the reaction system elongates the life of the catalyst.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16109779A JPS5683430A (en) | 1979-12-12 | 1979-12-12 | Preparation of pyrogallol |
US06/213,900 US4319054A (en) | 1979-12-12 | 1980-12-08 | Process for producing pyrogallol |
EP80107874A EP0031530B1 (en) | 1979-12-12 | 1980-12-12 | Process for producing pyrogallol |
DE8080107874T DE3067213D1 (en) | 1979-12-12 | 1980-12-12 | Process for producing pyrogallol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16109779A JPS5683430A (en) | 1979-12-12 | 1979-12-12 | Preparation of pyrogallol |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5683430A true JPS5683430A (en) | 1981-07-08 |
JPS6261008B2 JPS6261008B2 (en) | 1987-12-18 |
Family
ID=15728541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16109779A Granted JPS5683430A (en) | 1979-12-12 | 1979-12-12 | Preparation of pyrogallol |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5683430A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6242670A (en) * | 1985-08-20 | 1987-02-24 | Sumitomo Electric Ind Ltd | Image sensor output binarization system |
-
1979
- 1979-12-12 JP JP16109779A patent/JPS5683430A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6242670A (en) * | 1985-08-20 | 1987-02-24 | Sumitomo Electric Ind Ltd | Image sensor output binarization system |
Also Published As
Publication number | Publication date |
---|---|
JPS6261008B2 (en) | 1987-12-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS57123143A (en) | Production of glycolic ester | |
JPS55141417A (en) | Production of biphenyls | |
JPS5236609A (en) | Process for preparation of alcohol and carbon monoxide | |
JPS5683430A (en) | Preparation of pyrogallol | |
JPS5742654A (en) | Preparation of dimethyl oxalate | |
JPS5416452A (en) | Preparation of dis(amnomethyl) cyclohexane | |
JPS54117427A (en) | Preparation of alkyl-substituted aromatic compound | |
JPS577430A (en) | Preparation of pyrogallol | |
JPS52133914A (en) | Preparation of acetaldehyde | |
JPS57102840A (en) | Preparation of side chain acetoxylated xylene | |
JPS5625150A (en) | Production of 3,3-diaminodiphenyl sulfone | |
JPS5212121A (en) | Process for preparation of unsaturated diesters | |
JPS54138514A (en) | Preparation of pyruvic acid | |
JPS5788136A (en) | Preparation of pyrogallol | |
JPS53147039A (en) | Preparation of carboxylic acid ester of hydroxymethyl-substituted aromatic compound | |
JPS5791937A (en) | Preparation of pyrogallol | |
JPS5325504A (en) | Isolation of glycols | |
JPS5373528A (en) | Preparation of halogenated aromatic primary amine | |
JPS5735535A (en) | Preparation of acetal | |
JPS5427547A (en) | Preparation of o-acylated cyclohexane-1,3-dioneenols | |
JPS5750941A (en) | Preparation of carboxylic ester | |
JPS5368716A (en) | Preparation of methyl formate | |
JPS56161336A (en) | Preparation of acetaldehyde and acetic acid | |
JPS5242816A (en) | Process for preparation of carboxylic acid salts | |
JPS5398911A (en) | Preparation of dichlorobutenes |