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The synthesis and some reactions of thiophene sulfides

XVII. The synthesis and reactions of 2-mercapto-3-thenylidenecyclohexylamine and its zinc chelate

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reaction of some electrophilic reagents (bromine, acetyl chloride, and acetic anhydride) and of butyllithium on the zinc chelate of 2-mercapto-3-thenylidenecyclohexylamine (IIIa) is examined. Bromination and acetylation of IIIa lead to fission of the chelate ring and the formation of a complex of thienoisothiazolium bromide with ZnBr2 (VIII), and the corresponding dimienodithiocine (X). Butyllithium combines with the C=N double bond of the chelate ring (IIIa), with the formation of the chelate XIII.

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For part XVI, see [16].

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Gol'dfarb, Y.L., Kalik, M.A. The synthesis and some reactions of thiophene sulfides. Chem Heterocycl Compd 5, 354–359 (1969). https://doi.org/10.1007/BF00471143

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