GB999461A - Improvements in and relating to the production of alcohols - Google Patents
Improvements in and relating to the production of alcoholsInfo
- Publication number
- GB999461A GB999461A GB1840362A GB1840362A GB999461A GB 999461 A GB999461 A GB 999461A GB 1840362 A GB1840362 A GB 1840362A GB 1840362 A GB1840362 A GB 1840362A GB 999461 A GB999461 A GB 999461A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbon monoxide
- under
- pressure
- ruthenium
- trimethylamine
- 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
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
-
- 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
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/24—Nitrogen compounds
-
- 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
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/20—Carbonyls
-
- 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
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
-
- 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
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/821—Ruthenium
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Ruthenium carbonyl may be produced by heating a solution of a ruthernium salt of a monocarboxylic acid (e.g. stearic) in an inert organic solvent, e.g. a hydrocarbon to 200 DEG C. under a mixture of equal volumes of hydrogen and carbon monoxide at 240 ats., and then under the same conditions of temperature and pressure, with carbon monoxide alone. The precipitate formed is filtered under a nitrogen atmosphere, and the filtrate is concentrated to the desired bulk under a carbon monoxide atmosphere.ALSO:Alcohols are made from olefines by a process which comprises bringing a straight or branched chain aliphatic mono-olefin containing at most 10 carbon atoms and preferably at most 4 carbon atoms, carbon monoxide, water and a base compound, defined as a compound of one of the elements of Group Vb of the Periodic Table, for example nitrogen or phosphorus, each of which is in the trivalent form and each valency of which is attached to a carbon atom, into contact at elevated temperature and pressure with ruthenium carbonyl. It is preferable that the ruthenium carbonyl is produced in situ from a ruthenium salt of an aliphatic monocarboxylic acid. The preferred basic compound is trimethylamine. The process may be carried out in the presence of an inert organic solvent such as a hydrocarbon or an alcohol containing up to 4 carbon atoms. Examples of other suitable bases include N-n-butylpyrrolidine and tri-n-butylphosphine. In Example 1 a solution of ruthenium stearate in a petrol is heated under pressure of a mixture of equal volumes of hydrogen and carbon monoxide and thereafter under a pressure of carbon monoxide only. The product is filtered under a nitrogen blanket and the precipitate is washed with petrol. The filtrate and washings are bulked and the liquid is evaporated under a carbon monoxide atmosphere. To this solution there are added trimethylamine, water and methanol, together with propylene and the reaction mixture is heated under a pressure of carbon monoxide. From the reaction product n-butanol and isobutanol are obtained. In another example ruthenium stearate, trimethylamine, water, methanol and propylene are heated together at elevated temperature under pressure of carbon monoxide. From the reaction product n-butanol and isobutanol are isolated. In other examples ruthenium carbonyl as such is used as the catalyst and the bases employed are trimethylamine n-n-butylpyrrolidine and tri-n-butylphosphine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1840362A GB999461A (en) | 1962-05-14 | 1962-05-14 | Improvements in and relating to the production of alcohols |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1840362A GB999461A (en) | 1962-05-14 | 1962-05-14 | Improvements in and relating to the production of alcohols |
Publications (1)
Publication Number | Publication Date |
---|---|
GB999461A true GB999461A (en) | 1965-07-28 |
Family
ID=10111859
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1840362A Expired GB999461A (en) | 1962-05-14 | 1962-05-14 | Improvements in and relating to the production of alcohols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB999461A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4451679A (en) * | 1982-10-21 | 1984-05-29 | Texaco Inc. | Alcohols and aldehydes prepared from olefins and synthesis gas |
US4451680A (en) * | 1982-10-21 | 1984-05-29 | Texaco Inc. | Alcohols prepared from olefins and synthesis gas |
US4469895A (en) * | 1982-10-21 | 1984-09-04 | Texaco Inc. | Process for preparing alcohols from olefins and synthesis gas |
-
1962
- 1962-05-14 GB GB1840362A patent/GB999461A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4451679A (en) * | 1982-10-21 | 1984-05-29 | Texaco Inc. | Alcohols and aldehydes prepared from olefins and synthesis gas |
US4451680A (en) * | 1982-10-21 | 1984-05-29 | Texaco Inc. | Alcohols prepared from olefins and synthesis gas |
US4469895A (en) * | 1982-10-21 | 1984-09-04 | Texaco Inc. | Process for preparing alcohols from olefins and synthesis gas |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1002429A (en) | Process for the preparation of alcohols | |
US3458547A (en) | Preparation of irh3(p(r)3)2 compounds | |
GB995459A (en) | Process for the conversion of olefinic compounds | |
US3040090A (en) | Processes of making oxygenated organic compounds | |
US3560572A (en) | Process | |
US3515757A (en) | Organic compounds and processes | |
US4245115A (en) | Selective carbonylation of olefinically unsaturated hydrocarbons using palladium-arsine or -stibine catalysts | |
GB999461A (en) | Improvements in and relating to the production of alcohols | |
US3597460A (en) | Transition metal complexes | |
US4315993A (en) | Preparation of ethylene glycol | |
GB1254063A (en) | Hydroformylation process and specific phosphine containing catalysts for this process | |
US3766279A (en) | Production of alcohols | |
GB1275370A (en) | A process for producing methyl esters of linear saturated carboxylic acids from ethylene and methanol | |
ES406577A1 (en) | Working up hydroformylation mixtures | |
US2771478A (en) | Production of carboxylic acid esters | |
US2980741A (en) | Di-valent nickel acetylene reactions | |
DE69605256T2 (en) | Catalyst compositions | |
US3657354A (en) | Process for preparing alcohols and aldehydes from olefins | |
US3781351A (en) | Preparation of alpha-hydroyamides | |
US3697600A (en) | Preparation of a ketone and an aldehyde,by carbonylation of an olefin in the presence of a secondary alcohol | |
GB903589A (en) | Improvements in and relating to the hydroformylation of olefines | |
US3391212A (en) | Process for the preparation of olefins | |
US3546269A (en) | Method of preparing gamma-hydroxybutyronitrile | |
US3361829A (en) | Process for decobalting hydroformylation reaction mixtures | |
US2731504A (en) | Production of aliphatic alcohols from olefins |