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Telomerization of Ethylene with Carbon Tetrachloride Initiated byN-Chloroalkylamines

Authors :
Teruzo Asahara
Manabu Sen\={o}
Noritaka Ohtani
Source :
Bulletin of the Chemical Society of Japan. 46:3193-3197
Publication Year :
1973
Publisher :
The Chemical Society of Japan, 1973.

Abstract

By using various N-chloroalkylamines, the telomerization of ethylene with carbon tetrachloride was carried out in a stainless steel autoclave at 130 °C. It was found that the yields and the compositions of telomers varied widely according to the kinds and the structures of N-chloroalkylamines. When N-chloromonoalkylamines or N-chlorodialkylamines were used, the total yield of telomers was high compared with the case using N,N-dichloroalkylamines. In the presence of both N-chloromonoalkylamines and N-chlorodialky]amines, the total yield of telomers became higher and the greater part of the telomers was 1:1 adduct (n=1 telomer CCl3CH2CH2Cl) of ethylene with carbon tetrachloride.

Details

ISSN :
13480634 and 00092673
Volume :
46
Database :
OpenAIRE
Journal :
Bulletin of the Chemical Society of Japan
Accession number :
edsair.doi...........70673ea1bb41361507675924d3914c89
Full Text :
https://doi.org/10.1246/bcsj.46.3193