Oxidations of Alcohols, Aldehydes, and Diols Using NaBr and Selectfluor

Abstract

We present protocols for the oxidation of alcohols and aldehydes and for the oxidative cyclization of diols which use a combination of Selectfluor and NaBr. For most substrates, the optimal solvent system is a 1:1 mixture of CH 3 CN/H 2 O, but, in select cases, biphasic 1:1 mixtures of EtOAc/H 2 O or CH 2 Cl 2 /H 2 O are superior. This procedure is operationally simple, uses inexpensive and readily available reagents, and tolerates a variety of functional groups. Mechanistic studies suggest that the active oxidant is hypobromous acid, generated by the almost instantaneous oxidation of Br – by Selectfluor in an aqueous milieu.

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