Chen Ying, Fan Yiyao, Li Yanqiu, Yao Chunsuo
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, P. R. China.
J Org Chem. 2023 Aug 18;88(16):11460-11472. doi: 10.1021/acs.joc.3c00440. Epub 2023 Aug 1.
A facile and versatile protocol for the efficient synthesis of 3-aryl-2,3-dihydrobenzofuran (ADB) has been reported first. This reaction features the cyclization and aryl migration reaction of -hydroxystilbene in ethanol, which is mediated by an iodonium ion, under ambient conditions. A class of ADB was prepared efficiently in good to excellent yields. Mechanism investigation revealed that acids and alcohols facilitated aryl migration, but alkaline and non-alcohol solvents promoted β elimination. The practicality of this strategy was further substantiated by two scale-up reactions and demonstrated in efficient synthetic elaboration.
首次报道了一种简便通用的高效合成3-芳基-2,3-二氢苯并呋喃(ADB)的方法。该反应的特点是在环境条件下,由碘鎓离子介导的对羟基二苯乙烯在乙醇中的环化和芳基迁移反应。一类ADB以良好至优异的产率高效制备。机理研究表明,酸和醇促进芳基迁移,而碱和非醇溶剂促进β消除。该策略的实用性通过两个放大反应得到进一步证实,并在高效合成精细加工中得到体现。