JPS54132542A - Production of n-alkyl derivative of p-aminoacetophenone - Google Patents
Production of n-alkyl derivative of p-aminoacetophenoneInfo
- Publication number
- JPS54132542A JPS54132542A JP4040478A JP4040478A JPS54132542A JP S54132542 A JPS54132542 A JP S54132542A JP 4040478 A JP4040478 A JP 4040478A JP 4040478 A JP4040478 A JP 4040478A JP S54132542 A JPS54132542 A JP S54132542A
- Authority
- JP
- Japan
- Prior art keywords
- copper
- aminoacetophenone
- halogenoacetophenone
- dialkylamine
- mono
- 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: The reaction between a mono or dialkylamine and p-halogenoacetophenone is effected in the presence or absence of copper powder to produce readily title compound used as intermediate for dyes, pigments and agricultural chemicals in high yield.
CONSTITUTION: A mono- or dialkylamine and p-halogenoacetophenone as p-chloroacetophenone are heated with stirring in an airtight pressure reactor, wherein in order to accelerate reaction rate or lower the reaction temperature, a copper powder, or a copper compound as copper oxide, copper halides, is used as a catalyst to produce an N-alky derivative of p-aminoacetophenone. The reaction temperature is 120W300, preferably 150W260°C. The molar ratio of two raw materials is 2 or more of the formaer compound to 1 of the latter.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4040478A JPS54132542A (en) | 1978-04-07 | 1978-04-07 | Production of n-alkyl derivative of p-aminoacetophenone |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4040478A JPS54132542A (en) | 1978-04-07 | 1978-04-07 | Production of n-alkyl derivative of p-aminoacetophenone |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS54132542A true JPS54132542A (en) | 1979-10-15 |
Family
ID=12579719
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4040478A Pending JPS54132542A (en) | 1978-04-07 | 1978-04-07 | Production of n-alkyl derivative of p-aminoacetophenone |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS54132542A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1468994A1 (en) * | 1996-05-03 | 2004-10-20 | Ciba SC Holding AG | Process for preparing cyclic amine substituted phenyl-alkyl-ketones |
-
1978
- 1978-04-07 JP JP4040478A patent/JPS54132542A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1468994A1 (en) * | 1996-05-03 | 2004-10-20 | Ciba SC Holding AG | Process for preparing cyclic amine substituted phenyl-alkyl-ketones |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1536239A (en) | Production of uranium dioxide | |
JPS54132542A (en) | Production of n-alkyl derivative of p-aminoacetophenone | |
JPS5225733A (en) | Process for preparation of benzaldehydes | |
JPS5576891A (en) | Production of methoxysilane | |
JPS51133206A (en) | Process for preparation of alpha,omega-diiodopolyfluoroalkanes | |
JPS5559121A (en) | 1-halo-3-decyne compound | |
JPS5697245A (en) | Preparation of carboxylic acid | |
JPS55111468A (en) | Preparation of n-benzyl-tetrahydro isoquinoline derivative | |
JPS5758645A (en) | Preparation of carbonate | |
JPS5323966A (en) | Preparation of indoline | |
JPS57144235A (en) | Preparation of anthraquinone | |
JPS5725361A (en) | Production of copper phthalocyanine and/or derivative thereof | |
JPS5740447A (en) | Preparation of 3-nitro-4- lower alkoxy aniline | |
JPS55104242A (en) | Preparation of organic dinitrile compound | |
JPS56115776A (en) | Preparation of 2-bromo-trifluoromethylpyridine | |
JPS5430144A (en) | Preparation of isocamphane | |
ES465723A1 (en) | Process for the production of haloacylamides | |
JPS5673060A (en) | Preparation of indoel or indole derivative | |
JPS55136263A (en) | Preparation of 3-trifluoromethylpyridine | |
JPS57134473A (en) | Preparation of hexafluoropropylene oxide | |
JPS55112568A (en) | New oxo-barbituric acid derivative antigen and production | |
JPS5527015A (en) | Preparation of catalyst solution | |
JPS54136599A (en) | Production of ammonia | |
JPS6434929A (en) | Method for dehydrating reaction of ethanol | |
GB1330598A (en) | Process for the preparation of oxirane compounds |