GB891067A - Improvements in the production of alcohols and amines - Google Patents

Improvements in the production of alcohols and amines

Info

Publication number
GB891067A
GB891067A GB19341/60A GB1934160A GB891067A GB 891067 A GB891067 A GB 891067A GB 19341/60 A GB19341/60 A GB 19341/60A GB 1934160 A GB1934160 A GB 1934160A GB 891067 A GB891067 A GB 891067A
Authority
GB
United Kingdom
Prior art keywords
amines
carbon monoxide
olefines
water
production
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
GB19341/60A
Inventor
Hubert Kindler
Hans Georg Trieschmann
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
Application filed by BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB891067A publication Critical patent/GB891067A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/60Preparation of compounds containing amino groups bound to a carbon skeleton by condensation or addition reactions, e.g. Mannich reaction, addition of ammonia or amines to alkenes or to alkynes or addition of compounds containing an active hydrogen atom to Schiff's bases, quinone imines, or aziranes

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)

Abstract

A catalyst for use in the conversion of olefines, carbon monoxide and water to alcohols, and olefines, carbon monoxide, water and ammonia or primary or secondary amines to alkylated amines, comprises iron carbonyl and an amine, which form a complex in situ. Suitable amines for use in the catalyst are primary, secondary or tertiary amines either in the free state or as their salts. In the examples a catalyst consisting of N-n-butyl pyrrolidine and iron carbonyl is used for the production of butanol.ALSO:Alcohols or amines are formed by continuously reacting olefines, carbon monoxide and water or olefines, carbon monoxide, water and ammonia or a primary or secondary amine, respectively, at a temperature of 90 DEG C.-120 DEG C. and a carbon monoxide partial pressure of 2.0-7.0 atmospheres gauge, while using as catalysts complex iron carbonyl hydride compounds which are continuously formed during the reaction from iron pentacarbonyl and an amine. Under these conditions 12%-40% by weight of iron carbonyl compounds present are in the form of the pentacarbonyl. The iron carbonyl compound is usually added in the form of iron pentacarbonyl, but other carbonyls, e.g. the tetracarbonyl may be used. The process is used for the production of alcohols from olefines, carbon monoxide, e.g. propanol, butanol and pentanol and to the production of alkylated amines. Suitable primary and secondary amines for use in the production of alkylated amines are, for example, methylamine, dimethylamine, ethylamine, diethylamine, pyrrolidine, piperidine, aniline, p-phenylene diamine and also amines having additional functional groups, e.g. alanine, anthranilic acid and sulphanilic acid. In the examples propylene is reacted with carbon monoxide and water in the presence of iron carbonyl and N-n-butyl-pyrrolidine, to give butanol.
GB19341/60A 1959-06-05 1960-06-01 Improvements in the production of alcohols and amines Expired GB891067A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE891067X 1959-06-05

Publications (1)

Publication Number Publication Date
GB891067A true GB891067A (en) 1962-03-07

Family

ID=6842620

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19341/60A Expired GB891067A (en) 1959-06-05 1960-06-01 Improvements in the production of alcohols and amines

Country Status (1)

Country Link
GB (1) GB891067A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4292242A (en) * 1978-12-06 1981-09-29 Sri International Production of amines
US4317932A (en) * 1980-02-22 1982-03-02 W. R. Grace & Co. Preparation of secondary amines
US4322530A (en) * 1980-02-22 1982-03-30 W. R. Grace & Co. Alkylation of polyamines

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4292242A (en) * 1978-12-06 1981-09-29 Sri International Production of amines
US4317932A (en) * 1980-02-22 1982-03-02 W. R. Grace & Co. Preparation of secondary amines
US4322530A (en) * 1980-02-22 1982-03-30 W. R. Grace & Co. Alkylation of polyamines

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