Electron Donor‐Acceptor Complex‐Assisted Photochemical Conversion of O‐2‐Nitrobenzyl Protected Hydroxamates to Amides

The hydroxamic acid functionality is present in various medicinal agents and has attracted special interest for synthetic transformations in both organic and medicinal chemistry. The N−O bond cleavage of hydroxamic acid derivatives provides an interesting transformation for the generation of various products. We demonstrate, herein, that O‐benzyl‐type protected hydroxamic acids may undergo photochemical N−O bond cleavage, in the presence or absence of a catalyst, leading to amides. Although some O‐benzyl protected aromatic hydroxamates may be photochemically converted to amides in the presence of a base and anthracene as the catalyst, employing O‐2‐nitrobenzyl group allowed the smooth conversion of both aliphatic and aromatic hydroxamates to primary or secondary amides in good to excellent yields in the presence of an amine, bypassing the need of a catalyst. DFT and UV‐Vis studies supported the effective generation of an electron donor‐acceptor (EDA) complex between O‐2‐nitrobenzyl hydroxamates and amines, which enabled the successful product formation under these photochemical conditions. An extensive substrate scope was demonstrated, showcasing that both aliphatic and aromatic hydroxamates are compatible with this protocol, affording a wide variety of primary and secondary amides. An efficient photochemical protocol for the conversion of O‐2‐nitrobenzyl hydroxamates to primary or secondary amides was developed. The N−O bond cleavage was achieved under LED irradiation at 370 nm in the presence of an amine, suggesting the generation of an electron donor‐acceptor (EDA) complex, as confirmed by supplementary DFT and UV‐Vis studies.