GB375358A - Improvements in the manufacture of tribromoethylalcohol - Google Patents

Improvements in the manufacture of tribromoethylalcohol

Info

Publication number
GB375358A
GB375358A GB902731A GB902731A GB375358A GB 375358 A GB375358 A GB 375358A GB 902731 A GB902731 A GB 902731A GB 902731 A GB902731 A GB 902731A GB 375358 A GB375358 A GB 375358A
Authority
GB
United Kingdom
Prior art keywords
tribromoacetaldehyde
aluminium
tribromoethylalcohol
solution
manufacture
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
GB902731A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB902731A priority Critical patent/GB375358A/en
Publication of GB375358A publication Critical patent/GB375358A/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
    • C07C31/34Halogenated alcohols

Landscapes

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

Abstract

Tribromoethylalcohol is prepared by treating tribromoacetaldehyde with alkyl compounds of aluminium or aluminium halogenides in the presence of an indifferent organic solvent and decomposing the condensation product formed by means of water, preferably acidified by a mineral acid. In an example solutions of tribromoacetaldehyde and aluminium triethyletherate in ether are mixed, ethylene being evolved, the resulting mixture is heated and sulphuric acid is added to give a solution from which tribromoethyl alcohol is obtained. Tribromoacetaldehyde may also react with diethylaluminium iodide or ethylaluminium diiodide in which cases the ethereal solution of the tribromoethylalcohol is washed with aqueous sodium thiosulphate to remove any dissolved iodine.
GB902731A 1931-03-24 1931-03-24 Improvements in the manufacture of tribromoethylalcohol Expired GB375358A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB902731A GB375358A (en) 1931-03-24 1931-03-24 Improvements in the manufacture of tribromoethylalcohol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB902731A GB375358A (en) 1931-03-24 1931-03-24 Improvements in the manufacture of tribromoethylalcohol

Publications (1)

Publication Number Publication Date
GB375358A true GB375358A (en) 1932-06-24

Family

ID=9863958

Family Applications (1)

Application Number Title Priority Date Filing Date
GB902731A Expired GB375358A (en) 1931-03-24 1931-03-24 Improvements in the manufacture of tribromoethylalcohol

Country Status (1)

Country Link
GB (1) GB375358A (en)

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