Beilstein Journal of Organic Chemistry (Nov 2016)

Development of a continuous process for α-thio-β-chloroacrylamide synthesis with enhanced control of a cascade transformation

  • Olga C. Dennehy,
  • Valérie M. Y. Cacheux,
  • Benjamin J. Deadman,
  • Denis Lynch,
  • Stuart G. Collins,
  • Humphrey A. Moynihan,
  • Anita R. Maguire

DOI
https://doi.org/10.3762/bjoc.12.246
Journal volume & issue
Vol. 12, no. 1
pp. 2511 – 2522

Abstract

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A continuous process strategy has been developed for the preparation of α-thio-β-chloroacrylamides, a class of highly versatile synthetic intermediates. Flow platforms to generate the α-chloroamide and α-thioamide precursors were successfully adopted, progressing from the previously employed batch chemistry, and in both instances afford a readily scalable methodology. The implementation of the key α-thio-β-chloroacrylamide casade as a continuous flow reaction on a multi-gram scale is described, while the tuneable nature of the cascade, facilitated by continuous processing, is highlighted by selective generation of established intermediates and byproducts.

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