JPS5466629A - Preparation of dihydric phenol - Google Patents
Preparation of dihydric phenolInfo
- Publication number
- JPS5466629A JPS5466629A JP12966577A JP12966577A JPS5466629A JP S5466629 A JPS5466629 A JP S5466629A JP 12966577 A JP12966577 A JP 12966577A JP 12966577 A JP12966577 A JP 12966577A JP S5466629 A JPS5466629 A JP S5466629A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- phenol
- salt
- dihydric phenol
- mole
- 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
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PURPOSE: To obtain a dihydric phenol, e.g. catechol, etc., with high selectively, by direct oxidation of a phenol with a peroxide, e.g. H2O2, etc., using a hydroxycarboxylic acid as a catalyst.
CONSTITUTION: A phenol is oxidized with at least one type of a peroxide or its salt selected from an organic peracid, e.g. peracetic acid, perpropionic acid, etc., H2O2, and an organic hydroperoxide selectively to give a dihydric phenol, e.g. pyrocatechol, etc. α-Hydroxymonocarboxylic acid or its salt, e.g. gtdrixtusibyttruc acic, benzilic acid, etc. having two hydroxarbon groups at the carbib atin at tge α-position to the carboxyle group, etc. may be cited as the hydroxymonocarboxylic acid or its salt, and the amount is 10-15W10-10 mole, preferably 10-4W5×10-2 mole per mole of the phenol.
EFFECT: High catalytic activity and outstanding activity even in a very small amount.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12966577A JPS5466629A (en) | 1977-10-31 | 1977-10-31 | Preparation of dihydric phenol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12966577A JPS5466629A (en) | 1977-10-31 | 1977-10-31 | Preparation of dihydric phenol |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5466629A true JPS5466629A (en) | 1979-05-29 |
Family
ID=15015113
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12966577A Pending JPS5466629A (en) | 1977-10-31 | 1977-10-31 | Preparation of dihydric phenol |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5466629A (en) |
-
1977
- 1977-10-31 JP JP12966577A patent/JPS5466629A/en active Pending
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