GB999461A - Improvements in and relating to the production of alcohols - Google Patents

Improvements in and relating to the production of alcohols

Info

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
Application number
GB1840362A
Inventor
Graham Frederick Cox
Gordon Howard Whitfield
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB1840362A priority Critical patent/GB999461A/en
Publication of GB999461A publication Critical patent/GB999461A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/02Boron or aluminium; Oxides or hydroxides thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/24Nitrogen compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/20Carbonyls
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32Addition reactions to C=C or C-C triple bonds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium

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.
GB1840362A 1962-05-14 1962-05-14 Improvements in and relating to the production of alcohols Expired GB999461A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (3)

* Cited by examiner, † Cited by third party
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