Skip to main content
Log in

Chlorination of N-tritylproline methyl ester

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reaction of N-tritylproline methyl ester with tert-butyl hypochlorite gave 2,4-dichloro-2-methoxycarbonyl-5-pyrroline, which is readily converted to 2-methoxycarbonyl-4-chloropyrrole. The intermediate products were identified by Chromatographic mass spectrometry when the reaction was carried out at low temperatures.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature Cited

  1. A. V. Eremeev, F. D. Polyak, and é. é. Liepin'sh, Khim. Geterotsikl. Soedin., No. 5, 707 (1984).

    Google Scholar 

  2. A. Gordon and R. Ford, The Chemist's Guide [Russian translation], Mir, Moscow (1976), p. 306.

    Google Scholar 

  3. Z. Berustrin and D. Ben-Ishai, Tetrahedron,33, 881 (1977).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 894–896, July, 1988.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Polyak, F.D., Eremeev, A.V., Gavars, M.P. et al. Chlorination of N-tritylproline methyl ester. Chem Heterocycl Compd 24, 733–735 (1988). https://doi.org/10.1007/BF00633164

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00633164

Keywords

Navigation