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Reactions of thioepichlorohydrin and 3-chlorothietane with potassium thiobutoxide

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

Thioepichlorohydrin reacts with potassium thiobutoxide without ring expansion to form butyl thioglycidyl sulfide. Butyl allyl disulfide is formed from 3-chlorothietane and potassium thiotautoxide.

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Literature cited

  1. M. Sander, Monatsh. Chem.,96, 895 (1965).

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  2. B. A. Arbuzov, O. N. Nuretdiriova, and L. Z. Nikonova, Izv. Akad. Nauk SSSR, Ser. Khim., 167 (1969).

  3. R. Pearson and J. Songstad, J. Amer. Chem. Soc., 89, 1827 (1967); Usp. Khim.,38, 1223 (1969).

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  4. O. N. Nuretdinova, F. F. Guseva, and B. A. Arbuzov, Izv. Akad. Nauk SSSR, Ser. Khim., 2851 (1969).

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Authors and Affiliations

  1. A. E. Arbuzov Institute of Organic and Physical Chemistry, Academy of Sciences of the USSR, USSR

    O. N. Nuretdinova & B. A. Arbuzov

Authors
  1. O. N. Nuretdinova
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  2. B. A. Arbuzov
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 550–552, March, 1972.

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Nuretdinova, O.N., Arbuzov, B.A. Reactions of thioepichlorohydrin and 3-chlorothietane with potassium thiobutoxide. Russ Chem Bull 21, 505–506 (1972). https://doi.org/10.1007/BF00863183

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  • DOI: https://doi.org/10.1007/BF00863183

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