GB762421A - Process for the production of ketones - Google Patents
Process for the production of ketonesInfo
- Publication number
- GB762421A GB762421A GB19716/54A GB1971654A GB762421A GB 762421 A GB762421 A GB 762421A GB 19716/54 A GB19716/54 A GB 19716/54A GB 1971654 A GB1971654 A GB 1971654A GB 762421 A GB762421 A GB 762421A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ketone
- keto
- catalyst
- suspension
- hydrogen
- 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.)
- Expired
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/86—Chromium
- B01J23/868—Chromium copper and chromium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/65—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/03—Precipitation; Co-precipitation
- B01J37/031—Precipitation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises a process for the production of an aliphatic ketone by the reduction of an aliphatic 1,3-keto-alcohol containing from 4 to 6 carbon atoms with hydrogen at a partial pressure in the range 1-100 atmospheres and at a temperature in the range 100-200 DEG C. in the presence of a catalyst having a dehydrating and a hydrogenating effect. In a modification adapted as a continuous process the catalyst is suspended in the ketone and hydrogen is passed through the suspension. The reaction apparatus used to carry out the Fischer-Tropsch synthesis may, for example, be used in this modification, in which it is advantageous to use an excess of hydrogen which, after separation of the water and ketone vapours evolved in the reaction from it, can be recycled. It is also advantageous to add a quantity of the keto-alcohol which is substantially equivalent to the ketone and water which distills off from the suspension, continuously to the suspension. The catalyst advantageously consists of mixed metal oxides such as copper oxide-chromium oxide or zinc oxide-chromium oxide or of dehydrating and hydrogenation catalysts, such as, on the one hand, aluminium oxide, silica gel, or pumice and, on the other hand, nickel catalysts. The catalyst may be used as a stationary or fixed bed, e.g. it may be disposed in the tubes of a pipe or tube reactor or the reactor may be lined with catalytic materials. In examples: (1) methyl ethyl ketone is prepared from 3-keto butanol-1 in the presence of copper-chromite at 150-160 DEG C., the pressure being 40 atmospheres guage at the beginning of the reaction and 18.7 atmospheres gauge at the end; (2) methyl-isopropyl ketone is prepared from 2-methyl-3-keto-butanol-1 under similar conditions.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE762421X | 1954-06-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB762421A true GB762421A (en) | 1956-11-28 |
Family
ID=6667964
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19716/54A Expired GB762421A (en) | 1954-06-19 | 1954-07-06 | Process for the production of ketones |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB762421A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0276767A2 (en) * | 1987-01-28 | 1988-08-03 | BASF Aktiengesellschaft | Process for the preparation of ketones |
EP1440963A1 (en) * | 2003-01-24 | 2004-07-28 | Japan Energy Corporation | Production method of ketone compound |
US6838106B2 (en) | 2000-12-12 | 2005-01-04 | Takasago International Corporation | Warming composition for food and drink or for oral care preparation |
-
1954
- 1954-07-06 GB GB19716/54A patent/GB762421A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0276767A2 (en) * | 1987-01-28 | 1988-08-03 | BASF Aktiengesellschaft | Process for the preparation of ketones |
EP0276767A3 (en) * | 1987-01-28 | 1988-10-05 | Basf Aktiengesellschaft | Process for the preparation of ketones |
US4866210A (en) * | 1987-01-28 | 1989-09-12 | Basf Aktiengesellschaft | Preparation of ketones |
US6838106B2 (en) | 2000-12-12 | 2005-01-04 | Takasago International Corporation | Warming composition for food and drink or for oral care preparation |
EP1440963A1 (en) * | 2003-01-24 | 2004-07-28 | Japan Energy Corporation | Production method of ketone compound |
US7034188B2 (en) | 2003-01-24 | 2006-04-25 | Japan Energy Corporation | Production method of ketone compound |
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