Sterically Regulated α-Oxygenation of α-Bromocarbonyl Compounds Promoted Using 2-Aryl-1,3-dimethylbenzimidazolines and Air

[Image: see text] A debrominative oxygenation protocol has been developed for the conversion of α-bromo-α,α-dialkyl-substituted carbonyl compounds to their corresponding α-hydroxy analogues. For example, stirring a solution of α-bromoisobutyrophenone and 2-aryl-1,3-dimethylbenzimidazoline (BIH-Ar) at room temperature under an air atmosphere leads to the efficient formation of α-hydroperoxyisobutyrophenone, which can be converted to α-hydroxyisobutyrophenone using Me(2)S reduction. In contrast, reaction of α-bromoacetophenone under the same conditions produces the α-hydrogenated product acetophenone. α-Keto-alkyl and benzimidazolyl radicals (BI(•)-Ar), generated via dissociative electron transfer from BIH-Ar to α-bromoketone substrates, serve as key intermediates in the oxidation and reduction processes. The dramatic switch from hydrogenation to oxygenation is attributed to a steric effect of α-alkyl substituents, which causes hydrogen atom abstraction from sterically crowded BIH-Ar to α-keto-alkyl radicals to be slow and enable preferential reaction with molecular oxygen. Generation of the α-keto-alkyl radical and BI(•)-Ar intermediates in these process and their sterically governed hydrogen atom transfer reactions are supported by results arising from DFT calculations. Moreover, an electron spin resonance study showed that visible light irradiation of phenyl benzimidazoline (BIH-Ph) in the presence of molecular oxygen produces the benzimidazolyl radical (BI(•)-Ph). The addition of thiophenol into the reaction of α-bromoisobutyrophenone and BIH-Ph predominantly produced α-phenylthiolated isobutyrophenone even if a high concentration of molecular oxygen exists. Furthermore, the developed protocol was applied to other α-bromo-α,α-dialkylated carbonyl compounds.