Reactions of dichlorotriphenylphosphorane with bis(trimethylsilyl) peroxide in the presence of some organic compounds have been found to give chlorinated products. Aromatic hydrocarbons bearing electron-donating substituents give the corresponding monochloroarenes, while an enol silyl ether is converted into α-chloro ketone. The mechanism is briefly discussed.
CITATION STYLE
Shibata, K., Itoh, Y., Tokitoh, N., Okazaki, R., & Inamoto, N. (1991). Reaction of Dichlorotriphenylphosphorane with Bis(trimethylsilyl) Peroxide. A New Method for the Formation of Electrophilic Chlorine Source. Bulletin of the Chemical Society of Japan, 64(12), 3749–3751. https://doi.org/10.1246/bcsj.64.3749
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