GB1140570A - Process for the production of unsaturated alcohols by selective hydrogenation of the corresponding aldehydes and ketones - Google Patents
Process for the production of unsaturated alcohols by selective hydrogenation of the corresponding aldehydes and ketonesInfo
- Publication number
- GB1140570A GB1140570A GB2003266A GB2003266A GB1140570A GB 1140570 A GB1140570 A GB 1140570A GB 2003266 A GB2003266 A GB 2003266A GB 2003266 A GB2003266 A GB 2003266A GB 1140570 A GB1140570 A GB 1140570A
- Authority
- GB
- United Kingdom
- Prior art keywords
- weight
- hydrogenation
- catalyst
- ketones
- alcohol
- 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
- B01J23/80—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 zinc, cadmium or mercury
-
- 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
-
- 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
- B01J23/90—Regeneration or reactivation
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,140,570. Catalytic hydrogenation. CHEMISCHE WERKE HULS A.G. 6 May, 1966 [8 May, 1965], No. 20032/66. Heading C2C. [Also in Division B1] Preparation of olefinically unsaturated alcohols by selective hydrogenation of the corresponding unsaturated aldehydes or ketones in the gas phase at a temperature of 150‹ to 300‹ C. wherein a catalyst is used which has a cadmium content of 30 to 70% by weight, a copper content of 15 to 70% by weight and a magnesium content of 3 to 40% by weight based on the total weight of the activating constituents reckoned as the elements and excluding any carrier present, the proportion of any carrier material present being from 0 to 90% by weight on the total catalyst including carrier material. The catalyst materials, obtained by precipitation as carbonates or hydroxides of the metals, may be used in the form of pressure mouldings or supported on specified carriers and are thermally treated prior to or simultaneously with reduction in hydrogen before use. A number of unsaturated carbocyclic and acyclic unsaturated aldehydes and ketones are specified as suitable starting materials. The vaporized ketone or aldehyde is passed over the catalyst with 1500 1.hr. of hydrogen at or above atmospheric pressure to give the desired unsaturated alcohol as well as minor amounts of the corresponding saturated alcohol and related aldehyde as by-product. Crotyl alcohol is obtained, optionally in association with butanol and/or butyraldehyde, by hydrogenation of crotonaldehyde. 2-Ethylhexenol-1 is obtained, optionally in association with 2-ethylhexanol and 2-ethylhexanal by the hydrogenation of 2-ethylhexenal-1. 2,5 - Endomethylene - 1,2,5,6 - tetrahydrobenzyl alcohol is obtained by hydrogenating 2,5- endomethylene - 1,2,5,6 - tetrahydrobenzaldehyde-1.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEC35801A DE1230012B (en) | 1965-05-08 | 1965-05-08 | Process for the production of unsaturated alcohols by selective hydrogenation of the corresponding aldehydes or ketones |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1140570A true GB1140570A (en) | 1969-01-22 |
Family
ID=7021989
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2003266A Expired GB1140570A (en) | 1965-05-08 | 1966-05-06 | Process for the production of unsaturated alcohols by selective hydrogenation of the corresponding aldehydes and ketones |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE680705A (en) |
DE (1) | DE1230012B (en) |
GB (1) | GB1140570A (en) |
-
1965
- 1965-05-08 DE DEC35801A patent/DE1230012B/en active Pending
-
1966
- 1966-05-06 BE BE680705D patent/BE680705A/xx unknown
- 1966-05-06 GB GB2003266A patent/GB1140570A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE1230012B (en) | 1966-12-08 |
BE680705A (en) | 1966-10-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Hutchings et al. | Selectivity enhancement in the hydrogenation of α, β-unsaturated aldehydes and ketones using thiophene-modified catalysts | |
US4094914A (en) | Process for the production of divalent alcohols | |
US4212825A (en) | Aldol condensation and hydrogenation process using a catalyst of nickel and cobalt together with zinc oxide and another metal of groups VIII, IIb, IIIa, IVa and Va of the periodic table | |
GB1191113A (en) | Production of Saturated Carbonyl Compounds | |
US4049725A (en) | Method for preparing primary alcohols having alkyls branched at the second carbon | |
US4421938A (en) | Preparation of aldehydes | |
GB1428715A (en) | Manufacture of predominantly straight-chain aldehydes | |
US3491159A (en) | Process for the preparation of saturated aliphatic alcohols | |
GB1140570A (en) | Process for the production of unsaturated alcohols by selective hydrogenation of the corresponding aldehydes and ketones | |
GB1312076A (en) | Hydroformylation process | |
US3153068A (en) | Preparation of ketones | |
US2011317A (en) | Dehydrogenation of unsaturated alcohols | |
US3361828A (en) | Preparation of higher molecular weight ketones | |
GB1209242A (en) | Production of saturated aliphatic alcohols | |
DE875802C (en) | Process for the production of organic compounds containing oxygen | |
Komarewsky et al. | Synthesis of Olefin Hydrocarbons by Catalytic Condensation and Dehydration of Aliphatic Aldehydes | |
GB1289571A (en) | ||
DE869053C (en) | Process for the production of higher molecular weight glycols | |
US3189655A (en) | Dienals | |
GB1338419A (en) | Process for the manufacture of ketones | |
GB1145337A (en) | Production of cyclododecene | |
ES388468A1 (en) | Production of 2-ethylhexan-1-al | |
GB1144257A (en) | Hydrogenation of halogenated aromatic carbonyl compounds | |
GB949255A (en) | Hydrogenation of aldehydes at enhanced rate using platinum and ruthenium catalysts | |
Larkin | The vapor phase catalytic dehydrogenation of 1, 6-hexanediol |