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Reaction of 2-Chloro-5-(chloromethyl)thiophene with Monoethanolamine Vinyl Ether

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

At the alkylation of monoethanolamine vinyl ether with 2-chloro-5-(chloromethyl)thiophene in ethyl alcohol (60-70°C) a product of disubstitution and transvinylation, viz. N,N-bis(5-chloro-2-thienylmethyl)-N-(2-hydroxyethyl)ammonium chloride is formed. The analogous reaction in the absence of solvent proceeds with the formation of N-(5-chloro-2-thienylmethyl)-N-(2-vinyloxyethyl)amine.

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REFERENCES

  1. B. A. Trofimov, Heteroatomic Derivatives of Acetylene [in Russian], Nauka, Moscow (1981), p. 114.

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Authors and Affiliations

  1. Irkutsk A. E. Favorsky Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, 664033, Russia

    L. K. Papernaya, E. N. Deryagina & A. I. Albanov

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  1. L. K. Papernaya
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  2. E. N. Deryagina
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  3. A. I. Albanov
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Papernaya, L.K., Deryagina, E.N. & Albanov, A.I. Reaction of 2-Chloro-5-(chloromethyl)thiophene with Monoethanolamine Vinyl Ether. Chemistry of Heterocyclic Compounds 38, 1052–1054 (2002). https://doi.org/10.1023/A:1021292812502

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  • DOI: https://doi.org/10.1023/A:1021292812502

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