Synthetic Procedure for Azidoalcohols Utilizing Polymer-Supported Reagent
E. C. S. Brenelli*, J. A. Brenelli, R. C. L. Pinto
Universidade Federal Fluminense, Brazil
21. September 2005 (online)
β-Azidoalcohols were prepared from α-haloketones by using polystrene-based azide (PS-azide) and borohydride exchange resin (PS-BER) (20 examples). The azidations of α-haloketones 1 were carried out in the presence of PS-azide exchange resin at 30 °C for 30 minutes to give the corresponding α-azidoketones 2 in 68-95% yields. The resulting α-azidoketones 2 were reduced with PS-BER at 30 °C for 30 minutes to give α-aryl-β-azidoalcohols 3 in 78-96% yields.