GB975134A - Process for the production of fatty alcohols - Google Patents

Process for the production of fatty alcohols

Info

Publication number
GB975134A
GB975134A GB566961A GB566961A GB975134A GB 975134 A GB975134 A GB 975134A GB 566961 A GB566961 A GB 566961A GB 566961 A GB566961 A GB 566961A GB 975134 A GB975134 A GB 975134A
Authority
GB
United Kingdom
Prior art keywords
acids
fatty
fatty acid
alcohol
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
Application number
GB566961A
Inventor
Karl-Heinz Eisenlohr
Theodor Voeste
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.)
GEA Group AG
Original Assignee
Metallgesellschaft AG
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 Metallgesellschaft AG filed Critical Metallgesellschaft AG
Priority to GB566961A priority Critical patent/GB975134A/en
Publication of GB975134A publication Critical patent/GB975134A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/147Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • C07C29/149Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/17Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds
    • C07C29/177Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds with simultaneous reduction of a carboxy group

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A fatty alcohol is produced by the catalytic hydrogenation of a fatty acid, or a derivative thereof, at 200-350 DEG C. and 200-700 atm. in the presence of a known catalyst for the hydrogenation of carboxylic acid esters to alcohols, the material to be hydrogenated being continuously introduced into a reaction medium which consists almost entirely of the desired alcohol which has been saturated with hydrogen, so that the material is distributed uniformly almost instantaneously throughout a large excess of the alcohol. Fatty acid derivatives which may be used as starting materials are esters, anhydrides and lactones of fatty acids, oxyfatty acids with or without esterified hydroxy groups and free or esterified ketofatty acids. The preferred starting material is a symmetrical ester of the fatty acid, e.g. n-heptyl-n-heptoate or lauryl laurate. The preferred catalysts are copper/chromium oxide catalysts which may be modified by additional components, e.g. barium. Examples are given of the hydrogenation of coconut oil fatty oil acids, palm-kernel fatty acid and tallow oil fatty acids.
GB566961A 1961-02-15 1961-02-15 Process for the production of fatty alcohols Expired GB975134A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB566961A GB975134A (en) 1961-02-15 1961-02-15 Process for the production of fatty alcohols

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB566961A GB975134A (en) 1961-02-15 1961-02-15 Process for the production of fatty alcohols

Publications (1)

Publication Number Publication Date
GB975134A true GB975134A (en) 1964-11-11

Family

ID=9800428

Family Applications (1)

Application Number Title Priority Date Filing Date
GB566961A Expired GB975134A (en) 1961-02-15 1961-02-15 Process for the production of fatty alcohols

Country Status (1)

Country Link
GB (1) GB975134A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4517391A (en) * 1982-06-04 1985-05-14 Basf Aktiengesellschaft Continuous preparation of ethanol
US4804790A (en) * 1983-07-14 1989-02-14 Henkel Kommanditgesellschaft Auf Aktien Process for obtaining fatty alcohols from free fatty acids
US4942266A (en) * 1988-03-19 1990-07-17 Henkel Kommanditgesellschaft Auf Aktien Process for producing fatty alcohols and C3 diols by catalytic hydrogenation
US5180858A (en) * 1989-04-24 1993-01-19 Henkel Kommanditgesellschaft Auf Aktien Process for the catalytic hydrogenation of liquid fatty acid methyl esters
US5386066A (en) * 1991-12-23 1995-01-31 Sud-Chemie Ag Catalyst and process for hydrogenation of carboxylic acid alkyl esters to higher alcohols

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4517391A (en) * 1982-06-04 1985-05-14 Basf Aktiengesellschaft Continuous preparation of ethanol
US4804790A (en) * 1983-07-14 1989-02-14 Henkel Kommanditgesellschaft Auf Aktien Process for obtaining fatty alcohols from free fatty acids
US4942266A (en) * 1988-03-19 1990-07-17 Henkel Kommanditgesellschaft Auf Aktien Process for producing fatty alcohols and C3 diols by catalytic hydrogenation
US5180858A (en) * 1989-04-24 1993-01-19 Henkel Kommanditgesellschaft Auf Aktien Process for the catalytic hydrogenation of liquid fatty acid methyl esters
US5386066A (en) * 1991-12-23 1995-01-31 Sud-Chemie Ag Catalyst and process for hydrogenation of carboxylic acid alkyl esters to higher alcohols

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