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A kinetic study on the reactions of the cumyloxyl radical (CumO • ) with a series of alkanols and alkanediols has been carried out. Predominant hydrogen atom transfer (HAT) from the α-C–H bonds of these substrates, activated by the presence of the OH group, is observed. The comparable k H values measured for ethanol and 1-propanol and the increase in k H measured upon going from 1,2-diols to structurally related 1,3- and 1,4-diols is indicative of β-C–H deactivation toward HAT to the electrophilic CumO •, determined by the electron-withdrawing character of the OH group. No analogous deactivation is observed for the corresponding diamines, in agreement with the weaker electron-withdrawing character of the NH 2 group. The significantly lower k H values measured for reaction of CumO • with densely oxygenated methyl pyranosides as compared to cyclohexanol derivatives highlights the role of β-C–H deactivation. The contribution of torsional effects on reactivity is evidenced by the ∼2-fold increase in k H observed upon going from the trans isomers of 4- tert -butylcyclohexanol and 1,2- and 1,4-cyclohexanediol to the corresponding cis isomers. These results provide an evaluation of the role of electronic and torsional effects on HAT reactions from alcohols and diols to CumO •, uncovering moreover β-C–H deactivation as a relevant contributor in defining site selectivity.
Salamone et al. (2018) studied this question.