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Synthesis and some transformations of thiophene series sulfides

XIII. Structure of the compound of formula C10H7NS4 obtained from sodium 2-diethoxymethyl-3-thienylmercaptide

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The compound of formula C10H7N84, formed by the reaction of sodium-2-diethoxymethyl-3-thienylmercaptide with ammonia followed by acidification to pH 8 [1], is evidently bis(3-thiono-2-thienylidene)-dimethylamine (Ia). The action of primary amines on the thienylidenamine Ia gives N-substituted 3-mercapto-2-thienylidenimines (XIIa-c). With nickel acetate the azomethine XIIa forms an intramolecular complex (XIII).

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References

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For Part XII see [1].

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Gol'dfarb, Y.L., Kalik, M.A. & Kirmalova, M.L. Synthesis and some transformations of thiophene series sulfides. Chem Heterocycl Compd 3, 50–53 (1967). https://doi.org/10.1007/BF00944257

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  • DOI: https://doi.org/10.1007/BF00944257

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