Abstract
Reaction of thiols with dihaloalkanes in the system hydrazine hydrate-base leads to alkyl(chloroalkyl) sulfides with different positions of the chlorine atom with respect to sulfur. The developed one-step procedure for the synthesis of such unsymmetrical sulfides is most suitable for arenethiols and alkanethiols having a long polymethylene chain. The reaction mechanism is discussed.
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Russavskaya, N.V., Korchevin, N.A., Alekminskaya, O.V. et al. New Preparative Procedure for the Synthesis of Chloroalkyl Sulfides. Russian Journal of Organic Chemistry 38, 1445–1448 (2002). https://doi.org/10.1023/A:1022540002086
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DOI: https://doi.org/10.1023/A:1022540002086