Thiol-Triggered Tandem Dearomative Michael Addition/Intramolecular Henry Reaction of 2-Nitrobenzofurans: Access to Sulfur-Containing Polyheterocyclic Compounds
Jun-Rui Zhuo, Jian‐Qiang Zhao, Lei Yang, Yu-Lu Wu, Yan-Ping Zhang, Yong You, Zhen‐Hua Wang, Ming‐Qiang Zhou, Wei‐Cheng Yuan
Abstract
An efficient dearomative cyclization of 2-nitrobenzofurans via a thiol-triggered tandem Michael addition/intramolecular Henry reaction has been developed. A range of thiochromeno[3,2- b ]benzofuran-11-ols and tetrahydrothieno[3,2- b ]benzofuran-3-ols could be obtained in up to 99% yield and up to >20:1 dr. The valuable thiochromone fused benzofurans could be prepared with the reaction of 2-nitrobenzofurans and 2-mercaptobenzaldehyde via the tandem dearomative Michael addition/intramolecular Henry reaction/rearomatization/oxidative dehydrogenation process in a one-pot two-step operation. A mechanism for the reaction was tentatively proposed.