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).
Similar content being viewed by others
References
Ya. L. Gol'dfarb, M. A. Kalik, and M. L. Kirmalova, KhGS [Chemistry of Heterocyclic Compounds], 62, 1967.
R. Mecke, R. Mecke, and A. Lüttringhaus, Z. Naturforsch.,10b, 367, 1955.
A. B. Turner, Quart. Rev.,18, 358, 1964.
S. Gronowitz, Ark. kemi,13, 269, 1958.
Ya. L. Gol'dfarb, M. A. Kalik, and M. L. Kirmalova, Izv. AN SSSR, OKhN, 701, 1967.
K. Koehler, W. Sandstrom, and E. H. Cordes, J. Am. Chem. Soc.,86, 2413, 1964.
Ya. L. Gol'dfarb, M. A. Kalik, and M. L. Kirmalova, Izv. AN SSSR, ser. khim., 897, 1966.
Author information
Authors and Affiliations
Additional information
For Part XII see [1].
Rights and permissions
About this article
Cite this article
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
Issue Date:
DOI: https://doi.org/10.1007/BF00944257