JPS5535064A - Preparation of betaphenylethyl alcohol - Google Patents

Preparation of betaphenylethyl alcohol

Info

Publication number
JPS5535064A
JPS5535064A JP10924078A JP10924078A JPS5535064A JP S5535064 A JPS5535064 A JP S5535064A JP 10924078 A JP10924078 A JP 10924078A JP 10924078 A JP10924078 A JP 10924078A JP S5535064 A JPS5535064 A JP S5535064A
Authority
JP
Japan
Prior art keywords
catalyst
modified
preparation
raney nickel
nickel catalyst
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
Application number
JP10924078A
Other languages
Japanese (ja)
Inventor
Yasuo Tokito
Noriaki Yoshimura
Masuhiko Tamura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kuraray Co Ltd
Original Assignee
Kuraray Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kuraray Co Ltd filed Critical Kuraray Co Ltd
Priority to JP10924078A priority Critical patent/JPS5535064A/en
Publication of JPS5535064A publication Critical patent/JPS5535064A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PURPOSE: To obtain the title compound at a low catalyst cost in high yield, by hydrogenating phenylacetamide in the presence of a specific Raney nickel catalyst under specified conditions.
CONSTITUTION: Phenylacetaldehyde (P) is hydrogenated in the presence of (a) a Raney nickel catalyst, e.g. modified with Mo, modified with at least one type of metal selected from Cr, Mo, W, Re, Mn, Ti, Fe, and Co, and (b) water in an amount of 20wt% or more based on (P) at 0W65°C under a hydrogen pressure ≥ 5atm to give β-phenylethyl alcohol, e.g. in a 96% yield and a conversion of 99%. The catalyst is inexpensive and has a long life.
COPYRIGHT: (C)1980,JPO&Japio
JP10924078A 1978-09-05 1978-09-05 Preparation of betaphenylethyl alcohol Pending JPS5535064A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10924078A JPS5535064A (en) 1978-09-05 1978-09-05 Preparation of betaphenylethyl alcohol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10924078A JPS5535064A (en) 1978-09-05 1978-09-05 Preparation of betaphenylethyl alcohol

Publications (1)

Publication Number Publication Date
JPS5535064A true JPS5535064A (en) 1980-03-11

Family

ID=14505156

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10924078A Pending JPS5535064A (en) 1978-09-05 1978-09-05 Preparation of betaphenylethyl alcohol

Country Status (1)

Country Link
JP (1) JPS5535064A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4929773A (en) * 1988-09-07 1990-05-29 Hoechst Celanese Corporation Method of producing 1-(4'-isobutylphenyl)ethanol
US4968668A (en) * 1987-02-06 1990-11-06 Consortium Fur Elektrochemische Industrie Gmbh Alcohols having 3-methyl or 3,5-dimethyl or 3,5-dimethylphenyl groups, a process for their preparation and a fragrance composition containing same
EP0684251B1 (en) * 1994-05-06 1999-08-18 Bayer Ag Process for the preparation of alpha-D-glucopyranosido-1,6-mannit and -sorbit from alpha-D-glucopyranisido-1,6-fructose
CN104190436A (en) * 2014-07-29 2014-12-10 万华化学集团股份有限公司 Preparation method of catalyst, catalyst prepared by method and method for preparing beta-phenethyl alcohol by using catalyst

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4968668A (en) * 1987-02-06 1990-11-06 Consortium Fur Elektrochemische Industrie Gmbh Alcohols having 3-methyl or 3,5-dimethyl or 3,5-dimethylphenyl groups, a process for their preparation and a fragrance composition containing same
US4929773A (en) * 1988-09-07 1990-05-29 Hoechst Celanese Corporation Method of producing 1-(4'-isobutylphenyl)ethanol
EP0684251B1 (en) * 1994-05-06 1999-08-18 Bayer Ag Process for the preparation of alpha-D-glucopyranosido-1,6-mannit and -sorbit from alpha-D-glucopyranisido-1,6-fructose
CN104190436A (en) * 2014-07-29 2014-12-10 万华化学集团股份有限公司 Preparation method of catalyst, catalyst prepared by method and method for preparing beta-phenethyl alcohol by using catalyst

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