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A study of the reaction of sulfur with organic compounds

XVIII. The action of sulfur on alip-halogen derivatives of 1,2-diphenylethane, 1,2- diphenylethylene, and tetraphenylethane

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reactions of sulfur with alip-halogen derivatives of 1,2-diphenylethane, 1,2-diphenylethylene, and tetraphenylethane have been studied. A new method for the production of tetraphenylthiophene (from C6H5CHClCHClC6H5), benzothieno[3,2-b]benzothiophene (from C6H5CHClCCl2C6H5), and of 2-phenylbenzo[b] thiophene (from C6H5CHBrCHBrC6H5) has been developed. On being treated with sulfur, tetraphenyl-1,2-dichloroethane is converted into tetraphenylethylene. 1,2-Diphenylethylene reacts with sulfur in the presence of hydrogen bromide forming 2-phenylbenzo[b]thiophene and tetraphenylthiophene.

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For part XVII, see [1].

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Voronkov, M.G., Udre, V.É. A study of the reaction of sulfur with organic compounds. Chem Heterocycl Compd 6, 421–425 (1970). https://doi.org/10.1007/BF00478381

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  • DOI: https://doi.org/10.1007/BF00478381

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