Visible-light-mediated direct C3 alkylation of quinoxalin-2(1)-ones using alkanes

Due to the high C-H bond dissociation energy of alkanes, the utilization of alkanes as alkyl radical precursors for C-H functionalization of heteroarenes is synthetically captivating but practically challenging, especially under metal- and photocatalyst-free conditions. We report herein a mild and practical visible-light-mediated method for C-H alkylation of quinoxalin-2(1 H )-ones using trifluoroacetic acid as a hydrogen atom transfer reagent and air as an oxidant. This mild protocol was performed under metal- and photocatalyst-free circumstances and presented good functional-group tolerance as well as a broad substrate scope. Visible-light-mediated C-H alkylation of quinoxalin-2(1 H )-ones using trifluoroacetic acid as a hydrogen atom transfer reagent under metal- and photocatalyst-free conditions is reported.