GB659824A - Production of benzene hexachloride - Google Patents

Production of benzene hexachloride

Info

Publication number
GB659824A
GB659824A GB554/48A GB55448A GB659824A GB 659824 A GB659824 A GB 659824A GB 554/48 A GB554/48 A GB 554/48A GB 55448 A GB55448 A GB 55448A GB 659824 A GB659824 A GB 659824A
Authority
GB
United Kingdom
Prior art keywords
chlorination
extent
per cent
temperature
benzene
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
GB554/48A
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.)
Pennsylvania Salt Manufacturing Co
Original Assignee
Pennsylvania Salt Manufacturing Co
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 Pennsylvania Salt Manufacturing Co filed Critical Pennsylvania Salt Manufacturing Co
Publication of GB659824A publication Critical patent/GB659824A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/013Preparation of halogenated hydrocarbons by addition of halogens
    • C07C17/02Preparation of halogenated hydrocarbons by addition of halogens to unsaturated hydrocarbons

Landscapes

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

Abstract

Benzene hexachloride enriched in g -isomer is prepared by treating liquid benzene with chlorine in presence of actinic light at a temperature in the range 15-40 DEG C., discontinuing the chlorination after 20-50 per cent by volume of the benzene has been converted to benzene hexachloride, separating solid phase material from the solution at a temperature which is correlated with the extent of chlorination, and then recovering the g -isomer enriched product from the solution without further chlorination. When the extent of chlorination is 20 per cent the separation temperature used is 0 DEG \sB 10 DEG C., when the extent is 50 per cent the separation temperature is 30 DEG \sB 10 DEG C., and these two conditions should be maintained in a linear relationship for intermediate values. In the examples: (1) the extent of chlorination was 43-45 per cent and the separation temperature about 25 DEG C.; (2) the extent was 20 per cent and the separation temperature 0 DEG C.; the chlorination temperature in both cases was just below 40 DEG C. The Specification as open to inspection under Sect. 91 comprises a process in which an inert solvent may be present in the reaction and in which higher separation temperatures and lower chlorination temperatures may be employed. An example is given of the process employing acetic acid as solvent. This subject-matter does not appear in the Specification as accepted.
GB554/48A 1947-04-04 1948-01-07 Production of benzene hexachloride Expired GB659824A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US659824XA 1947-04-04 1947-04-04

Publications (1)

Publication Number Publication Date
GB659824A true GB659824A (en) 1951-10-31

Family

ID=22066478

Family Applications (1)

Application Number Title Priority Date Filing Date
GB554/48A Expired GB659824A (en) 1947-04-04 1948-01-07 Production of benzene hexachloride

Country Status (1)

Country Link
GB (1) GB659824A (en)

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