JPS54128539A - Preparation of acrylophenone derivative - Google Patents
Preparation of acrylophenone derivativeInfo
- Publication number
- JPS54128539A JPS54128539A JP3529378A JP3529378A JPS54128539A JP S54128539 A JPS54128539 A JP S54128539A JP 3529378 A JP3529378 A JP 3529378A JP 3529378 A JP3529378 A JP 3529378A JP S54128539 A JPS54128539 A JP S54128539A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- derivative
- chloride
- friedel
- moles
- 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 prepare the title compound useful as an intermediate of medicines, by the Friedel-Crafts condensation reaction of a benzene derivative with methacroyl chloride using said denzene derivative as solvent, in the presence of aluminum chloride as catalsyt, at low temperature.
CONSTITUTION: The compound III (R is alkyl), e.g. 4'-2-dimethyl-acrylophenone, etc., is prepared by the Friedel-Crafts condensation reaction of a benzene derivative I (R is alkyl) (5W20 moles), e.g. toluene, etc., with methacryloyl chloride II (1 mole) in the presence of aluminum chloride (1.0W1.2 moles) as catalyst, pref. at -15 -+20°C. The compound I acts as a reaction solvent.
EFFECT: The objective compound can be easily produced in high yield without producing intramolecular ring-closing product.
USE: The compound I wherein R is methyl, is an intermediate of an excellent anti- spasmodic agent.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3529378A JPS54128539A (en) | 1978-03-29 | 1978-03-29 | Preparation of acrylophenone derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3529378A JPS54128539A (en) | 1978-03-29 | 1978-03-29 | Preparation of acrylophenone derivative |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS54128539A true JPS54128539A (en) | 1979-10-05 |
Family
ID=12437716
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3529378A Pending JPS54128539A (en) | 1978-03-29 | 1978-03-29 | Preparation of acrylophenone derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS54128539A (en) |
-
1978
- 1978-03-29 JP JP3529378A patent/JPS54128539A/en active Pending
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