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Reaction of 3,3,4,4-tetracyanopyrrolidines with primary alcohols and amines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

2,5-Substituted 3,3,4,4-tetracyanopyrrolidines react with primary alcohols in the presence of an excess of a base or with the base itself. 2-(N-Arylideneamino)-5-alkoxy-3,4-dicyanopyrroles are formed as a result of the reactions with alcohols, and 2,5-diamino-1-R-3,4-dicyanopyrroles are formed as the result of the reaction with primary aliphatic amines.

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Literature Cited

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Authors and Affiliations

  1. I. N. Ul'yanov Chuvashsk State University, 428015, Cheboksary

    O. E. Nasakin, A. N. Lyshchikov, P. M. Lukin, A. Kh. Bulai, V. A. Tafeenko & P. A. Sharbatyan

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  1. O. E. Nasakin
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  2. A. N. Lyshchikov
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  3. P. M. Lukin
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  4. A. Kh. Bulai
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  5. V. A. Tafeenko
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  6. P. A. Sharbatyan
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1502–1507, November, 1991.

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Nasakin, O.E., Lyshchikov, A.N., Lukin, P.M. et al. Reaction of 3,3,4,4-tetracyanopyrrolidines with primary alcohols and amines. Chem Heterocycl Compd 27, 1212–1217 (1991). https://doi.org/10.1007/BF00471746

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  • DOI: https://doi.org/10.1007/BF00471746

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