33951-13-2Relevant articles and documents
KINETICS AND MECHANISM OF HOMOLYTIC TRANSFORMATIONS OF 1,3-OXATHIOLANES IN CARBON TETRACHLORIDE
Batyrbaev, N. A.,Zorin, V. V.,Zlot-skii, S. S.,Rakhmankulov, D. L.
, p. 368 - 372 (2007/10/02)
In carbon tetrachloride in the presence of tert-butyl peroxide at 120-150 deg C 1,3-oxathiolanes are converted into chloroethyl thioacylates.The kinetics were studied and an unbranched radical-chain mechanism for the formation of the chlorothio esters through the formation of 2-chloro-1,3-oxathiolanes is proposed.The controlling stage of the process is the abstraction of a hydrogen atom from the substrate by the trichloromethyl radical.The effect of the nature of the heteroatom and substituent at position 2 of the heterocycle on the reactivity of the substrate was dtermined.