JPS5520729A - Preparation of keto-alcohol - Google Patents

Preparation of keto-alcohol

Info

Publication number
JPS5520729A
JPS5520729A JP9368578A JP9368578A JPS5520729A JP S5520729 A JPS5520729 A JP S5520729A JP 9368578 A JP9368578 A JP 9368578A JP 9368578 A JP9368578 A JP 9368578A JP S5520729 A JPS5520729 A JP S5520729A
Authority
JP
Japan
Prior art keywords
keto
alcohol
diol
palladium
carrier
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
Application number
JP9368578A
Other languages
Japanese (ja)
Other versions
JPS6116256B2 (en
Inventor
Nobuhiro Tamura
Yohei Fukuoka
Yoshio Suzuki
Setsuo Yamamatsu
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP9368578A priority Critical patent/JPS5520729A/en
Publication of JPS5520729A publication Critical patent/JPS5520729A/en
Publication of JPS6116256B2 publication Critical patent/JPS6116256B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE: To obtain the title compound useful as an intermediate for medicines or synthesis in high yeild selectively, by bringing an α,β-diol into contact with a palladium or platinum catalyst at a low temperature under oxidizing conditions.
CONSTITUTION: A ≥3C α,β-diol of formula I: (R is alkyl, vinyl, or aromatic group) is brough into contact with a palladium or platinum catalyst in the presence of a molecular oxygen-containing gas at 0W200°C, preferably normal temperature to 150°C, to give an α-keto-alcohol of formula II. The amount of oxygen is 1.5 times that is stoichiometrically required for the reaction. The catalyst may be a metal, however, preferably supported on a carrier, e.g. active carbon, silica, or alumina, and the amount is 0.5W10 wt.% based on the carrier.
COPYRIGHT: (C)1980,JPO&Japio
JP9368578A 1978-08-02 1978-08-02 Preparation of keto-alcohol Granted JPS5520729A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9368578A JPS5520729A (en) 1978-08-02 1978-08-02 Preparation of keto-alcohol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9368578A JPS5520729A (en) 1978-08-02 1978-08-02 Preparation of keto-alcohol

Publications (2)

Publication Number Publication Date
JPS5520729A true JPS5520729A (en) 1980-02-14
JPS6116256B2 JPS6116256B2 (en) 1986-04-28

Family

ID=14089255

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9368578A Granted JPS5520729A (en) 1978-08-02 1978-08-02 Preparation of keto-alcohol

Country Status (1)

Country Link
JP (1) JPS5520729A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017536386A (en) * 2014-12-05 2017-12-07 アディッソ・フランス・エス.エー.エス.Adisseo France S.A.S. Catalytic oxidation of but-3-ene-1,2-diol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017536386A (en) * 2014-12-05 2017-12-07 アディッソ・フランス・エス.エー.エス.Adisseo France S.A.S. Catalytic oxidation of but-3-ene-1,2-diol

Also Published As

Publication number Publication date
JPS6116256B2 (en) 1986-04-28

Similar Documents

Publication Publication Date Title
JPS557239A (en) Preparation of dicarboxylic diester
JPS5520729A (en) Preparation of keto-alcohol
JPS577254A (en) Catalyst for reforming of methanol
JPS565471A (en) Preparation of ethylene oxide
JPS5639045A (en) Recovery of benzylbenzoate
JPS54138514A (en) Preparation of pyruvic acid
JPS56104839A (en) Preparation of acetic acid and/or methyl acetate
JPS5346912A (en) Preparation of acetyl halides
JPS5692832A (en) Preparation of aromatic polycarboxylic acid
JPS5377029A (en) Slkylation of phenol
JPS55133321A (en) Preparation of perfluoro-2-butene
JPS5791936A (en) Preparation of ortho-methylated phenolic compound
JPS5444605A (en) Preparation of methanol
JPS554325A (en) Preparation of phenyl acetate and ketone
JPS5356612A (en) Purification of maleic acid anhydride
JPS5791984A (en) Preparation of lactone
JPS5728026A (en) Preparation of aromatic dicarboxylic acid
JPS5616423A (en) Preparation of alkenylbenzene
JPS54163509A (en) Preparation of methacrolein
JPS5359639A (en) Preparation of terephthalic acid
JPS5762231A (en) Preparation of oxygen-containing 2c compound from synthesis gas
JPS5645428A (en) Preparation of o-alkylated phenol
JPS56104838A (en) Preparation of acetic acid and/or methyl acetate
JPS56131529A (en) Preparation of styrene
JPS5592338A (en) Preparation of methyl ethyl ketone