Metal-Free <i>ortho</i>-Selective C–H Borylation of 2-Phenylthiopyridines Using BBr₃

Abstract

A novel route for <i>ortho</i>-selective C-H borylation of 2-phenylthiopyridines using BBr₃ as the boron source under metal-free conditions has been reported. The reaction exhibited site exclusivity, and the synthesized aryl boronates were freely converted to various useful intermediates. Thus, this facile method would be beneficial to synthesize structurally diversified phenylthioethers derivatives and other materials containing boron-nitrogen coordination.