JPS54128542A - Preparation of 3-cyanocatechol derivative - Google Patents
Preparation of 3-cyanocatechol derivativeInfo
- Publication number
- JPS54128542A JPS54128542A JP3410978A JP3410978A JPS54128542A JP S54128542 A JPS54128542 A JP S54128542A JP 3410978 A JP3410978 A JP 3410978A JP 3410978 A JP3410978 A JP 3410978A JP S54128542 A JPS54128542 A JP S54128542A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- derivative
- reacting
- aqueous medium
- basic aqueous
- 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 prepare the title compound in high selectivity and yield, useful as a raw material of medicine, pesticide, and dyestuff, by reacting 3-formylocatechol derivative with an N-containing compound in a basic aqueous medium, in the presence of a metal compound.
CONSTITUTION: The compound II (X is H, lower alkyl, lower alkoxy, halogen) is prepared by reacting a 3-formlycatechol derivative I with an N-containing compound selected from ammonia, urea and inorganic ammonium salts (e.g. NH4Cl, (NH4)2SO4, etc.), in a basic aqueous medium at pH9.5W11.5, in the presence of more than equi-molar amount, based on the compound I, of oxide, hydroxide, chloride, sulfate, and/or acetate of a metal selected from Cu, Fe, Mn, Ni and Zn.
EFFECT: The objective compound can be obtained by single state reaction in a short time.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3410978A JPS54128542A (en) | 1978-03-27 | 1978-03-27 | Preparation of 3-cyanocatechol derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3410978A JPS54128542A (en) | 1978-03-27 | 1978-03-27 | Preparation of 3-cyanocatechol derivative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS54128542A true JPS54128542A (en) | 1979-10-05 |
JPS5721272B2 JPS5721272B2 (en) | 1982-05-06 |
Family
ID=12405103
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3410978A Granted JPS54128542A (en) | 1978-03-27 | 1978-03-27 | Preparation of 3-cyanocatechol derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS54128542A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0237929A1 (en) * | 1986-03-11 | 1987-09-23 | F. Hoffmann-La Roche Ag | 3,5-Disubstituted pyrocatechol derivatives |
WO2014013512A1 (en) * | 2012-07-19 | 2014-01-23 | Laurus Labs Private Limited | Improved process for preparation of 2,3-dihydroxy benzonitrile |
CN112374973A (en) * | 2020-11-20 | 2021-02-19 | 成都伊诺达博医药科技有限公司 | Synthesis method of drug intermediate 4-bromo-2, 3-dihydroxybenzaldehyde |
-
1978
- 1978-03-27 JP JP3410978A patent/JPS54128542A/en active Granted
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0237929A1 (en) * | 1986-03-11 | 1987-09-23 | F. Hoffmann-La Roche Ag | 3,5-Disubstituted pyrocatechol derivatives |
WO2014013512A1 (en) * | 2012-07-19 | 2014-01-23 | Laurus Labs Private Limited | Improved process for preparation of 2,3-dihydroxy benzonitrile |
US9567292B2 (en) | 2012-07-19 | 2017-02-14 | Laurus Labs Private Limited | Process for preparation of 2,3-dihydroxy benzonitrile |
CN112374973A (en) * | 2020-11-20 | 2021-02-19 | 成都伊诺达博医药科技有限公司 | Synthesis method of drug intermediate 4-bromo-2, 3-dihydroxybenzaldehyde |
CN112374973B (en) * | 2020-11-20 | 2023-06-30 | 成都伊诺达博医药科技有限公司 | Synthesis method of drug intermediate 4-bromo-2, 3-dihydroxybenzaldehyde |
Also Published As
Publication number | Publication date |
---|---|
JPS5721272B2 (en) | 1982-05-06 |
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