JPS57169440A - Preparation of arylacetone derivative - Google Patents
Preparation of arylacetone derivativeInfo
- Publication number
- JPS57169440A JPS57169440A JP56055017A JP5501781A JPS57169440A JP S57169440 A JPS57169440 A JP S57169440A JP 56055017 A JP56055017 A JP 56055017A JP 5501781 A JP5501781 A JP 5501781A JP S57169440 A JPS57169440 A JP S57169440A
- Authority
- JP
- Japan
- Prior art keywords
- compound shown
- compound
- acetylacetone
- give
- formula
- 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 obtain the titled compound industrially advantageously useful as an intermediate for a sympathetic stimulant, an anticoagulant, etc., by deacetylating a reaction product obtained by reacting an aryl halide derivative with acetylacetone in the presence of cuprous halide.
CONSTITUTION: A compound shown by the formula Ar-X (Ar is substituted or unsubstituted aromatic group; X is halogen) is reacted with acetylacetone in the presence of cuprous halide, and, preferably further a base as well in an aprotic polar solvent at 80W120°C, to give a compound shown by the formulaI. This compound is then deacetylated under an alkali condition to give a compound shown by the formula II such as 2-amino-1-arylpropanols, 6-aryl-2,3,5-trioxotetrahydropyrans, etc. useful as an intermediate for the above-mentioned drugs. This process evables the two-stage reactions in the same container, the operations of the reactions and isolation are simple, and reagents are also inexpensive.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56055017A JPS57169440A (en) | 1981-04-14 | 1981-04-14 | Preparation of arylacetone derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56055017A JPS57169440A (en) | 1981-04-14 | 1981-04-14 | Preparation of arylacetone derivative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57169440A true JPS57169440A (en) | 1982-10-19 |
JPH0161093B2 JPH0161093B2 (en) | 1989-12-27 |
Family
ID=12986890
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56055017A Granted JPS57169440A (en) | 1981-04-14 | 1981-04-14 | Preparation of arylacetone derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57169440A (en) |
-
1981
- 1981-04-14 JP JP56055017A patent/JPS57169440A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0161093B2 (en) | 1989-12-27 |
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