A novel method for the conversion of halide anion to the positive halogen by nitrobenzenesulfonyl peroxide. Application to oxyhalogenation of olefin.
…, H Mochizuki, T Suzuki, N Kamigata
Index: Yoshida, Masato; Mochizuki, Hideki; Suzuki, Takashi; Kamigata, Nobumasa Bulletin of the Chemical Society of Japan, 1990 , vol. 63, # 12 p. 3704 - 3706
Full Text: HTML
Citation Number: 12
Abstract
Bromide and chloride anions could be readily oxidized into positive halogens by treating with p-nitrobenzenesulfonyl peroxide. The positive halogens, thus formed, reacted with olefins to give epihalonium ions, which were trapped by oxygen nucleophiles inter-or intramolecularly to afford oxyhalogenated compounds.
Related Articles:
2-Diethylaminoethyl esters of 1, 3-disubstituted propane-2-carboxylic acids
[Collection of Czechoslovak Chemical Communications, , vol. 52, # 10 p. 2534 - 2544]
[Journal of Organic Chemistry, , vol. 55, # 10 p. 2997 - 2998]
[Dalton Transactions, , vol. 41, # 19 p. 5805 - 5815]