Alcohols and 1,2-diols oxidation by o -iodoxybenzoic acid (IBX) has been examined by 1 H-NMR spectroscopy. Reversible formation of reactive intermediates, iodic esters 5, has been observed, and their structures in DMSO- d 6 solution have been defined as 10-I-4 axial alkoxyiodinane oxides by comparison of the chemical shift difference data with those obtained for Dess−Martin periodinane (DMP)−alcoholate and −diolate adducts. The dichotomous behavior exhibited by IBX and DMP with 1,2-diols can be explained in terms of the different architecture of the reactive intermediates involved in the oxidation. With aliphatic alcohols, kinetic evidences support a two-step reaction mechanism involving a fast pre-equilibrium step leading to 5, followed by a rate-determining disproportionation step. With electronically activated benzyl alcohol, the attainment of pre-equilibrium is largely dependent on initial water concentration as a consequence of a particularly high k 2 value. The influence of the alcohol structure on measured equilibrium ( K eq ) and rate constants ( k 2 ) and the effect of water on the overall reaction rate are discussed.
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Munari et al. (1996) studied this question.