Beilstein Journal of Organic Chemistry (Aug 2018)

Bi-mediated allylation of aldehydes in [bmim][Br]: a mechanistic investigation

  • Mrunesh Koli,
  • Sucheta Chatterjee,
  • Subrata Chattopadhyay,
  • Dibakar Goswami

DOI
https://doi.org/10.3762/bjoc.14.193
Journal volume & issue
Vol. 14, no. 1
pp. 2198 – 2203

Abstract

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The inexpensive room temperature ionic liquid (RTIL), [bmim][Br] has been found to be a superior medium for the Bi-mediated Barbier-type allylation of aldehydes compared to other conventional solvents. It plays the dual role of a solvent and a metal activator enabling higher yields of the products in a shorter reaction time using stoichiometric/near-stoichiometric amounts of reagents. Plausibly, [bmim][Br] activates Bi metal by a charge transfer mechanism. The 1H VT-NMR studies suggested that both the allylating species, allylbismuth dibromide and diallylbismuth bromide, are generated in situ.

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