Beilstein Journal of Organic Chemistry (Jan 2021)

Synthesis of aryl 2-bromo-2-chloro-1,1-difluoroethyl ethers through the base-mediated reaction between phenols and halothane

  • Yukiko Karuo,
  • Ayaka Kametani,
  • Atsushi Tarui,
  • Kazuyuki Sato,
  • Kentaro Kawai,
  • Masaaki Omote

DOI
https://doi.org/10.3762/bjoc.17.9
Journal volume & issue
Vol. 17, no. 1
pp. 89 – 96

Abstract

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An efficient and convenient method for the synthesis of structurally unique and highly functionalized aryl 2-bromo-2-chloro-1,1-difluoroethyl ethers has been developed. This approach exhibits a broad reaction scope, a simple operation and without the need of any expensive transition-metal catalyst, highly toxic or corrosive reagents. Notably, we demonstrate the potential utility of halothane for the synthesis of aryl gem-difluoroalkyl ethers containing the bromochloromethyl group.

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