Hypervalent Iodine(III)‐Promoted Metal‐Free S–H Activation: An Approach for the Construction of S–S, S–N, and S–C Bonds

Abstract

Abstract The activation of the sulfur atom of thiols with (diacetoxyiodo)benzene (DIB) has been explored in the preparation of symmetrical disulfides and sulfenamides. Disulfides can be produced in excellent yields (75–95 %) upon treatment of thiols with DIB. The reaction was complete in less than five minutes at room temperature. Aliphatic, aromatic, and heteroaromatic thiols are compatible with this transformation. Moreover, heteroaromatic disulfides obtained from heteroaromatic thiols further reacted with a nucleophilic amine in the presence of a base to provide the corresponding sulfenamides in fair to good yields (43–90 %) in a one‐pot fashion. The methodology was successfully extended to indole as a representative electron‐rich aromatic compound, which allowed successful construction of a S–C bond in one pot. The key benefits of this reaction include lower toxicity, low cost of DIB reagent, and mild reaction conditions (room temperature, undried solvents and open flask).