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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2015 Volume 25, Issue 6, Pages 440–442 (Mi mendc2438)

This article is cited in 8 papers

Communications

A novel synthesis of 2-alkyl(aryl)pyrrolidines from proline via 2,3-diphenylhexahydropyrrolo[2,1-b]oxazoles

V. S. Moshkin, V. Ya. Sosnovskikh

Department of Chemistry, Ural Federal University, Ekaterinburg, Russian Federation

Abstract: Diphenyloxapyrrolizidines, products of the reaction between proline and benzaldehyde, are convenient building blocks for synthesizing 2-substituted pyrrolidines. The opening of their oxazolidine ring by treatment with Grignard reagents has been performed and conditions for subsequent removal of the N-hydroxyethyl moiety have been found. Though the yields are moderate (36–42%), the suggested synthesis of 2-alkyl(aryl)pyrrolidines is rather simple since it does not require purification of intermediate products and is easy scalable.

Language: English

DOI: 10.1016/j.mencom.2015.11.014



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