JPS55102527A - Preparation of aldehyde or ketone - Google Patents
Preparation of aldehyde or ketoneInfo
- Publication number
- JPS55102527A JPS55102527A JP963979A JP963979A JPS55102527A JP S55102527 A JPS55102527 A JP S55102527A JP 963979 A JP963979 A JP 963979A JP 963979 A JP963979 A JP 963979A JP S55102527 A JPS55102527 A JP S55102527A
- Authority
- JP
- Japan
- Prior art keywords
- aldehyde
- ketone
- oxidation
- alcohol
- 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
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 an aldehyde or ketone selectively and in high yield, by the oxidation of the corresponding alcohol with a peroxide in the presence of a catalyst comprising a noble metal (compound) of the VIII group in the periodic table.
CONSTITUTION: An aldehyde such as n-heptyl aldehyde and citral, or a ketone is obtained by the oxidation of a primary alcohol, such as n-heptanol and geraniol, or a secondary alcohol with peroxides, such as H2O2, in the presence of a catalyst comprising a noble metal of the VIII group in the periodic table, such as Ru, Pt and Pd or its compound such as RuCl3, if necessary in the presence of a solvent, preferably at 0W150°C. The amount of the catalyst used is preferably 0.001W0.1 gram atom as the metal atom to one mole of the alcohols.
EFFECT: An aldehyde or ketone can be obtained without breaking the structure of the starting compound even in the case wherein a C=C unsaturated bond or a structure susceptible to oxidation is present in the starting alcohol.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP963979A JPS55102527A (en) | 1979-02-01 | 1979-02-01 | Preparation of aldehyde or ketone |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP963979A JPS55102527A (en) | 1979-02-01 | 1979-02-01 | Preparation of aldehyde or ketone |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS55102527A true JPS55102527A (en) | 1980-08-05 |
Family
ID=11725789
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP963979A Pending JPS55102527A (en) | 1979-02-01 | 1979-02-01 | Preparation of aldehyde or ketone |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS55102527A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4480135A (en) * | 1982-07-28 | 1984-10-30 | Anic S.P.A. | Process for oxidizing alcohols to aldehydes and/or ketones |
WO2004060844A1 (en) * | 2003-01-07 | 2004-07-22 | National Institute Of Advanced Industrial Science And Technology | PROCESS FOR PRODUCING α,ß-UNSATURATED CARBONYL COMPOUND |
-
1979
- 1979-02-01 JP JP963979A patent/JPS55102527A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4480135A (en) * | 1982-07-28 | 1984-10-30 | Anic S.P.A. | Process for oxidizing alcohols to aldehydes and/or ketones |
WO2004060844A1 (en) * | 2003-01-07 | 2004-07-22 | National Institute Of Advanced Industrial Science And Technology | PROCESS FOR PRODUCING α,ß-UNSATURATED CARBONYL COMPOUND |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS55102527A (en) | Preparation of aldehyde or ketone | |
JPS52139011A (en) | Synthesis of linear unsaturated alcohols | |
JPS5273804A (en) | Production of ethylalcohol | |
JPS53141219A (en) | Preparation of polyethylene glycollic acid | |
JPS5524106A (en) | Preparation of methyl methacrylate | |
JPS5748931A (en) | Preparation of carbonyl compound | |
JPS5398923A (en) | Preparation of hydroxyacetic acid | |
JPS5550473A (en) | Production of ketones | |
JPS52133914A (en) | Preparation of acetaldehyde | |
JPS5377010A (en) | Preparation of hydroxypivalic acid | |
JPS5726634A (en) | Preparation of aromatic alcohol | |
JPS54138514A (en) | Preparation of pyruvic acid | |
JPS55147234A (en) | Preparation of (+)-2-isopropyl-5-methyl-cyclohexanone | |
JPS53144544A (en) | Production of cyclohexanols | |
JPS52148037A (en) | Preparation of per-#-toluylic acid | |
JPS5271430A (en) | Preparation of alkylphenylsulfide | |
JPS5398934A (en) | Preparation of 3-alkoxy-4-hydroxybenzaldehyde | |
JPS5398917A (en) | Preparation of ethyleneglycol monoether | |
JPS5315350A (en) | Preparation of 2-hydroxy-1,4-naphthoquinone | |
JPS532430A (en) | Preparation of resorcin | |
JPS52105108A (en) | Preparation of primary alcohols | |
JPS5626829A (en) | Preparation of phenylacetaldehyde dialkyl acetal | |
JPS53124219A (en) | Preparation of derivative of 5-oxocarboxylic acid | |
JPS53149950A (en) | Preparation of cyclohexyl carbinols | |
JPS5788136A (en) | Preparation of pyrogallol |