GB922374A - Production of alcohols - Google Patents

Production of alcohols

Info

Publication number
GB922374A
GB922374A GB8207/61A GB820761A GB922374A GB 922374 A GB922374 A GB 922374A GB 8207/61 A GB8207/61 A GB 8207/61A GB 820761 A GB820761 A GB 820761A GB 922374 A GB922374 A GB 922374A
Authority
GB
United Kingdom
Prior art keywords
water
catalyst
additives
lactam
compounds
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
GB8207/61A
Inventor
Nikolaus Von Kutepow
Hubert Kindler
Karl Eisfeld
Karl Dettke
Helmut Jenne
Hans Detzer
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik 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
Priority claimed from DEB57065A external-priority patent/DE1114796B/en
Priority claimed from DEB57101A external-priority patent/DE1114797B/en
Application filed by BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB922374A publication Critical patent/GB922374A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/02Monohydroxylic acyclic alcohols
    • C07C31/125Monohydroxylic acyclic alcohols containing five to twenty-two carbon atoms
    • 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
    • C07C29/14Preparation 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 a —CHO group
    • C07C29/141Preparation 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 a —CHO group 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
    • C07C29/32Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions without formation of -OH groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/02Monohydroxylic acyclic alcohols
    • C07C31/08Ethanol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/02Monohydroxylic acyclic alcohols
    • C07C31/10Monohydroxylic acyclic alcohols containing three carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/13Monohydroxylic alcohols containing saturated rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/18Monohydroxylic alcohols containing only six-membered aromatic rings as cyclic part
    • C07C33/20Monohydroxylic alcohols containing only six-membered aromatic rings as cyclic part monocyclic

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)

Abstract

Catalysts used for the reaction between olefines, carbon monoxide and water to produce alcohols comprise an iron carbonyl, preferably iron pentacarbonyl, an amine, preferably a tertiary amine such as N-n-butylpyrrolidine, water and an optionally substituted ether, thioether, nitrile, lactam, carboxylic acid amide, a compound containing a sulphoxide group or two or more of such compounds. The additives are preferably present in an amount of 1-20% by weight based on the total weight of the three components forming the catalyst.ALSO:Alcohols having 3-7 carbon atoms are obtained from olefines having 2-6 carbon atoms, carbon monoxide and water at a temperature of 60-130 DEG C. in the presence of a complex catalyst consisting of iron carbonyl, an amine and water and an optionally substituted ether, thioether, nitrile, lactam, carboxylic acid amide, a compound containing a sulphoxide group or two or more of such compounds. The amine is preferably a tertiary one, e.g. N-n-butyl pyrrolidine. Among suitable additives specified are those of formula R1XR2, in which X is oxygen or sulphur and R1 and R2 are aliphatic, cycloaliphatic, araliphatic or aromatic radicals containing 1-12 carbon atoms substituted, for example, by esterified carboxylic groups, etherified hydroxy groups, esterified hydroxy groups, carboxylic groups, hydroxy groups and nitrile groups, and compounds of formula R3COYR4, in which Y is oxygen or a group NR5 in which R5 is hydrogen, an aliphatic, cycloaliphatic, araliphatic or aromatic radical both hetero atoms being members of a heterocyclic ring having 5-13 atoms as ring members and R3 and R4 together represent a polymethylene radical with 3-11 carbon atoms which together with -CO-Y- form a heterocyclic ring having 5-13 ring members. Suitable compounds of formula R3COYR4 are, for example, pyrrolidone, caprolactam, caprylic lactam, lauric lactam, N-methylpyrrolidone, and N-butylcaprolactam. Other suitable additives are N-mono- and N-disubstituted carbonamides, e.g. dimethyl and diethyl formamide, N.N-dimethyl acetamide, N.N-diethylbutyramide and benzoic and dimethyl amide. The additives are usually present in an amount of 1-20% by weight based on the total of the three components forming the catalyst and may be added during or after the formation of the catalyst. In the examples propylene is reacted with carbon monoxide and water in the presence of a catalyst comprising iron pentacarbonyl, N-butyl pyrrolidine and various additives as specified above to give a mixture of butanols. Specification 704,136 is referred to.
GB8207/61A 1960-03-15 1961-03-07 Production of alcohols Expired GB922374A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEB57065A DE1114796B (en) 1960-03-15 1960-03-15 Process for the production of alcohols from olefins
DEB57101A DE1114797B (en) 1960-03-18 1960-03-18 Process for the production of alcohols from olefins

Publications (1)

Publication Number Publication Date
GB922374A true GB922374A (en) 1963-03-27

Family

ID=25965596

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8207/61A Expired GB922374A (en) 1960-03-15 1961-03-07 Production of alcohols

Country Status (1)

Country Link
GB (1) GB922374A (en)

Similar Documents

Publication Publication Date Title
ES316768A1 (en) Procedure for the preparation of a new polyamide. (Machine-translation by Google Translate, not legally binding)
GB1070322A (en) Process for the preparation of 6-formyloxy caproic acids and derivatives thereof
GB967718A (en) N-substituted azaspiranes
IE41052L (en) Use of an amine salt of p-alkylbenzenesulphonic acid in crop¹protection
GB1276142A (en) 0,4-dialkyl-1,4-cyclohexane derivatives
GB922374A (en) Production of alcohols
GB1079314A (en) Process for preparing n-vinyl compounds
GB962857A (en) Process for the production of imides
GB1425597A (en) Urocanic acid derivatives
ES271134A1 (en) Method of producing dibenzo (a, d) cyclohepta (1, 4) dienes
SE9000420D0 (en) A PROCESS FOR THE MANUFACTURE OF N, N-DISUBSTITUTEDMANDELAMINDES
GB771151A (en) Method for the preparation of aminoacyl-anilides
DE3060541D1 (en) Process for the production of n-substituted acryl amides
JPS55122750A (en) Production of aminonitrile
GB985107A (en) Process for the manufacture of thermoplastic polyureas
GB1107572A (en) Process for the manufacture of n-acyl taurides
SU133892A1 (en) The method of obtaining hdoracetamidine hydrochloride
BR8101325A (en) PROCESS FOR PREPARING ALPHA-KETO-CARBOXYLIC ACID N-ACYLAMIDES
CH614704A5 (en) Process for the preparation of novel N-(p-fluorobenzoylpropyl)-4-piperidylamids
GB840880A (en) Improvements in or relating to the synthesis of acrylonitrile
JPS5569622A (en) Production of fiber-hard-finishing agent
GB734305A (en) Process for the poly-condensation of methylene-, alkylidene- and aralkylidene-bis-halogeno-carboxylic acid amides
GB912788A (en) Phenylpiperazinylacyl anilines
GB847205A (en) A process for the manufacture of ethylenimine derivatives and novel ethylenimine derivatives
GB976531A (en) Process for making polypyrrolidone