JPS5527147A - Preparation of carboxylic acid having aryl substituent - Google Patents
Preparation of carboxylic acid having aryl substituentInfo
- Publication number
- JPS5527147A JPS5527147A JP9985578A JP9985578A JPS5527147A JP S5527147 A JPS5527147 A JP S5527147A JP 9985578 A JP9985578 A JP 9985578A JP 9985578 A JP9985578 A JP 9985578A JP S5527147 A JPS5527147 A JP S5527147A
- Authority
- JP
- Japan
- Prior art keywords
- carboxylic acid
- alcohol
- water
- hydrogen fluoride
- aryl substituent
- 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 the title carboxylic acid at a low cost in a one-step reaction without using an expensive metal catalyst, by reacting an alcohol having an aryl substituent with carbon monoxide and water in the presence of hydrogen fluoride as a catalyst.
CONSTITUTION: An alcohol, e.g. α-(4-isobutyl)ethand, having an aryl substitutent of the formula (R1 and R2 are H or 1-4C alkyl groups; R3, R4, and R5 are H, halogen, 1W4C alkyl, phenyl groups, etc.) is dissolved in a solvent, e.g. n-hexane, and reacted with carbon monoxide and water in the presence of hydrogen fluoride as a catalyst at 0W50°C and 10W100 kg/cm2G to give the objective carboxylic acid. The molar ratios of the hydrogen fluoride and water to the alcohol are preferably 10W 80:1 and 1.5W5:1, respectively.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9985578A JPS5527147A (en) | 1978-08-16 | 1978-08-16 | Preparation of carboxylic acid having aryl substituent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9985578A JPS5527147A (en) | 1978-08-16 | 1978-08-16 | Preparation of carboxylic acid having aryl substituent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5527147A true JPS5527147A (en) | 1980-02-27 |
Family
ID=14258408
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9985578A Pending JPS5527147A (en) | 1978-08-16 | 1978-08-16 | Preparation of carboxylic acid having aryl substituent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5527147A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62263140A (en) * | 1986-05-09 | 1987-11-16 | Daicel Chem Ind Ltd | Production of alpha-phenylpropionic acid derivative |
US4929773A (en) * | 1988-09-07 | 1990-05-29 | Hoechst Celanese Corporation | Method of producing 1-(4'-isobutylphenyl)ethanol |
WO1991003453A1 (en) * | 1989-09-07 | 1991-03-21 | Daicel Chemical Industries, Ltd. | Optically active 2-(alkyl-substituted phenyl)-propionic acid derivative and optical resolution of (±)-1-methyl-3-phenylpropylamine |
EP0421759A2 (en) * | 1989-10-05 | 1991-04-10 | Hoechst Celanese Corporation | Method for producing 1-indanone derivatives |
US5166418A (en) * | 1990-06-04 | 1992-11-24 | Hoechst Celanese Corporation | Method for producing ibuprofen |
US5179229A (en) * | 1992-04-24 | 1993-01-12 | Hoechst Celanese Corporation | Preparation of 2,2-diorgano-3-arylpropionic acids and esters thereof |
WO2002079134A1 (en) * | 2001-02-13 | 2002-10-10 | F. Hoffmann-La-Roche Ag | Process for the manufacture of phenylacetic acid derivatives |
WO2003074144A3 (en) * | 2002-03-06 | 2004-03-04 | Molecularnature Ltd | Process for scavenging phytochemicals |
US8779200B2 (en) | 2009-02-25 | 2014-07-15 | Council Of Scientific & Industrial Research | Microwave induced single step green synthesis of some novel 2-aryl aldehydes and their analogues |
-
1978
- 1978-08-16 JP JP9985578A patent/JPS5527147A/en active Pending
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62263140A (en) * | 1986-05-09 | 1987-11-16 | Daicel Chem Ind Ltd | Production of alpha-phenylpropionic acid derivative |
JPH0625088B2 (en) * | 1986-05-09 | 1994-04-06 | ダイセル化学工業株式会社 | Process for producing α-phenylpropionic acid derivative |
US4929773A (en) * | 1988-09-07 | 1990-05-29 | Hoechst Celanese Corporation | Method of producing 1-(4'-isobutylphenyl)ethanol |
EP0441979B1 (en) * | 1989-09-07 | 1996-01-31 | Daicel Chemical Industries, Ltd. | Optically active 2-(alkyl-substituted phenyl)-propionic acid derivative and optical resolution of ( )-1-methyl-3-phenylpropylamine |
WO1991003453A1 (en) * | 1989-09-07 | 1991-03-21 | Daicel Chemical Industries, Ltd. | Optically active 2-(alkyl-substituted phenyl)-propionic acid derivative and optical resolution of (±)-1-methyl-3-phenylpropylamine |
EP0421759A2 (en) * | 1989-10-05 | 1991-04-10 | Hoechst Celanese Corporation | Method for producing 1-indanone derivatives |
US5012007A (en) * | 1989-10-05 | 1991-04-30 | Varadaraj Elango | Method for producing 1-indanone derivatives |
US5166418A (en) * | 1990-06-04 | 1992-11-24 | Hoechst Celanese Corporation | Method for producing ibuprofen |
US5179229A (en) * | 1992-04-24 | 1993-01-12 | Hoechst Celanese Corporation | Preparation of 2,2-diorgano-3-arylpropionic acids and esters thereof |
WO2002079134A1 (en) * | 2001-02-13 | 2002-10-10 | F. Hoffmann-La-Roche Ag | Process for the manufacture of phenylacetic acid derivatives |
JP2004524358A (en) * | 2001-02-13 | 2004-08-12 | エフ.ホフマン−ラ ロシュ アーゲー | Method for producing phenylacetic acid derivative |
WO2003074144A3 (en) * | 2002-03-06 | 2004-03-04 | Molecularnature Ltd | Process for scavenging phytochemicals |
US8779200B2 (en) | 2009-02-25 | 2014-07-15 | Council Of Scientific & Industrial Research | Microwave induced single step green synthesis of some novel 2-aryl aldehydes and their analogues |
US8981152B2 (en) | 2009-02-25 | 2015-03-17 | Council Of Scientific & Industrial Research | Microwave induced single step green synthesis of some novel 2-aryl aldehydes and their analogues |
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