GB745946A - Improvements in the production of saturated ketones - Google Patents
Improvements in the production of saturated ketonesInfo
- Publication number
- GB745946A GB745946A GB2199553A GB2199553A GB745946A GB 745946 A GB745946 A GB 745946A GB 2199553 A GB2199553 A GB 2199553A GB 2199553 A GB2199553 A GB 2199553A GB 745946 A GB745946 A GB 745946A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chromium
- acid
- activated
- copper
- hydrogenation
- 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
-
- 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
-
- 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
- C07C45/66—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 by dehydration
-
- 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
- C07C45/67—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 isomerisation; by change of size of the carbon skeleton
- C07C45/673—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 isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton
-
- 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
- C07C45/67—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 isomerisation; by change of size of the carbon skeleton
- C07C45/68—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 isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—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 isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
A process for the production of saturated ketones comprises hydrogenating a ketol, preferably one with a tertiary hydroxyl group, in the presence of a hydrogenation catalyst and a free acid which remains a free acid in the presence of hydrogen at elevated temperature. Suitable catalysts are metals of the first or eighth sub group of the periodic system which may be activated by chromium, alkali metals, magnesium, boron or alumina and may be deposited on a carrier such as pumice, silica gel, kieselguhr, charcoal, coke, chamotte or porcelain. Non-volatile acids derived from phosphorus or boron, such as phosphoric, boric, phosphomolybdic, phosphotungstic and borotungstic acids or borylphosphate are preferred, but volatile organic acids such as formic, acetic and propionic acids and aromatic acids such as benzoic, phenylacetic and phthalic acids are also suitable. The carrier-free hydrogenation catalyst may be added to the ketol in which at least 5 per cent of an organic acid is dissolved, or the catalyst or the inorganic acid may be suspended on a carrier. Hydrogenation at high pressure, e.g. 100 to 300 atmospheres, is preferred. The process may be effected intermittently or batchwise. Temperatures of about 150 DEG to 300 DEG C. are suitable. Ketols obtainable by condensation with aqueous alkali hydroxides such as pentanolone-2,4, diacetone alcohol), 3-methyl-pentanolone-2,4, heptanolone-2,4, undecanolone-2,4, benzoylisopropanol and (1-hydroxypropyl)-cyclohexanone can be hydrogenated. In examples diacetone alcohol is hydrogenated (1) in an autoclave with acetic acid and a chromium-activated to give acetone, isopropanol, hexone, methylpentanol and components of higher boiling-point; (2) as in (1), in the presence of added water, to give hexone and cleavage products; (3) by passage with hydrogen under pressure through a heated tube containing a catalyst comprising copper and chromium with phosphoric acid on silica gel, to give acetone, isopropanol, hexone and mesityl oxide; (4) by passage with hydrogen through a heated tube containing boric acid, phosphoric acid, copper, nickel and chromium (obtained by mixing borylphosphate and a CuNi-hydrogenation catalyst, activated with chromium) to give acetone, isopropanol, methyl pentanone and hexone; (5) by passage under pressure with hydrogen through a heated tube charged with a mixture of coke, phosphoric acid, Na2H2P2O7, trimetaphosphate and Madrell salt and a hydrogenation catalyst containing cooper, nickel, chromium and kieselguhr to give hexone and higher-boiling materials.ALSO:As hydrogenation catalysts for use in a process of preparing a saturated ketone by hydrogenation of a ketol in the presence of a free acid which remains a free acid in the presence of hydrogen at elevated temperature (see Group IV(b)), there are specified metals of the first or eighth group of the periodic system which may be activated by chromium, alkali metals, magnesium, boron or alumina and may be deposited on a carrier such as pumice, silica gel, kieselguhr, charcoal, coke, chamotte or porcelain. In examples there are employed (1) and (2) a carrier-free copper catalyst activated by chromium, (3) a catalyst containing copper, phosphoric acid, chromium and silica gel, (4) a mixture of boric acid, phosphoric acid, copper, nickel, chromium and kieselguhr obtained by mixing boryl phosphate and a Cu-Ni-hydrogenation catalyst activated with chromium (5) a mixture of coke phosphoric acid Na2H2P2O7, trimetaphosphate and Madrell salt and a hydrogenation catalyst containing copper, nickel, chromium and kieselguhr.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2199553A GB745946A (en) | 1953-08-10 | 1953-08-10 | Improvements in the production of saturated ketones |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2199553A GB745946A (en) | 1953-08-10 | 1953-08-10 | Improvements in the production of saturated ketones |
Publications (1)
Publication Number | Publication Date |
---|---|
GB745946A true GB745946A (en) | 1956-03-07 |
Family
ID=10172228
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2199553A Expired GB745946A (en) | 1953-08-10 | 1953-08-10 | Improvements in the production of saturated ketones |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB745946A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0276767A2 (en) * | 1987-01-28 | 1988-08-03 | BASF Aktiengesellschaft | Process for the preparation of ketones |
WO2012039839A1 (en) * | 2010-09-23 | 2012-03-29 | Celanese International Corporation | Production of alcohols |
CN102548944A (en) * | 2009-10-09 | 2012-07-04 | 花王株式会社 | Process for producing 2-alkylcycloalkanone |
US8460405B2 (en) | 2010-02-02 | 2013-06-11 | Celanese International Corporation | Ethanol compositions |
US8541633B2 (en) | 2010-02-02 | 2013-09-24 | Celanese International Corporation | Processes for producing anhydrous ethanol compositions |
US8668750B2 (en) | 2010-02-02 | 2014-03-11 | Celanese International Corporation | Denatured fuel ethanol compositions for blending with gasoline or diesel fuel for use as motor fuels |
US8728179B2 (en) | 2010-02-02 | 2014-05-20 | Celanese International Corporation | Ethanol compositions |
US8747492B2 (en) | 2010-02-02 | 2014-06-10 | Celanese International Corporation | Ethanol/fuel blends for use as motor fuels |
US8932372B2 (en) | 2010-02-02 | 2015-01-13 | Celanese International Corporation | Integrated process for producing alcohols from a mixed acid feed |
-
1953
- 1953-08-10 GB GB2199553A patent/GB745946A/en not_active Expired
Cited By (17)
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 |
CN102548944B (en) * | 2009-10-09 | 2014-12-10 | 花王株式会社 | Process for producing 2-alkylcycloalkanone |
CN102548944A (en) * | 2009-10-09 | 2012-07-04 | 花王株式会社 | Process for producing 2-alkylcycloalkanone |
EP2487150A1 (en) * | 2009-10-09 | 2012-08-15 | Kao Corporation | Process for producing 2-alkylcycloalkanone |
EP2487150A4 (en) * | 2009-10-09 | 2013-03-20 | Kao Corp | Process for producing 2-alkylcycloalkanone |
US8541633B2 (en) | 2010-02-02 | 2013-09-24 | Celanese International Corporation | Processes for producing anhydrous ethanol compositions |
US8460405B2 (en) | 2010-02-02 | 2013-06-11 | Celanese International Corporation | Ethanol compositions |
US8668750B2 (en) | 2010-02-02 | 2014-03-11 | Celanese International Corporation | Denatured fuel ethanol compositions for blending with gasoline or diesel fuel for use as motor fuels |
US8728179B2 (en) | 2010-02-02 | 2014-05-20 | Celanese International Corporation | Ethanol compositions |
US8747492B2 (en) | 2010-02-02 | 2014-06-10 | Celanese International Corporation | Ethanol/fuel blends for use as motor fuels |
US8747493B2 (en) | 2010-02-02 | 2014-06-10 | Celanese International Corporation | Ethanol compositions |
US8858659B2 (en) | 2010-02-02 | 2014-10-14 | Celanese International Corporation | Processes for producing denatured ethanol |
US8932372B2 (en) | 2010-02-02 | 2015-01-13 | Celanese International Corporation | Integrated process for producing alcohols from a mixed acid feed |
US9447005B2 (en) | 2010-02-02 | 2016-09-20 | Celanese International Corporation | Processes for producing anhydrous ethanol compositions |
WO2012039839A1 (en) * | 2010-09-23 | 2012-03-29 | Celanese International Corporation | Production of alcohols |
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