Al-Zoubi Raed M, Al-Jammal Walid K, Ferguson Michael J, Murphy Graham K
Department of Chemistry, Jordan University of Science and Technology P.O. Box 3030 Irbid 22110 Jordan
Department of Chemistry, Gunning-Lemieux Chemistry Centre, University of Alberta Edmonton Alberta T6G2G2 Canada.
RSC Adv. 2021 Sep 8;11(48):30069-30077. doi: 10.1039/d1ra05730h. eCollection 2021 Sep 6.
A facile and efficient synthesis of 7-iodobenzo[]furan derivatives a highly regioselective tandem α-arylation/intramolecular -arylation of 5-substituted-1,2,3-triiodobenzenes and benzylketones is described. Remarkably, the α-arylation coupling reactions initiate exclusively at the least sterically-hindered position of the triiodoarene, which results in a highly chemoselective transformation. The highest yields were observed in reactions between electron-poor 1,2,3-triiodoarenes and electron-rich benzylketones, yet the optimized reaction conditions were found to be tolerant to a wide range of different functional groups. This unprecedent synthesis of 7-iodobenzo[]furans from 1,2,3-triiodobenzenes is scalable, general in scope, and provides easy access to valuable precursors for other chemical transformations.
本文描述了一种简便高效的7-碘苯并呋喃衍生物的合成方法,即5-取代-1,2,3-三碘苯与苄基酮的高度区域选择性串联α-芳基化/分子内β-芳基化反应。值得注意的是,α-芳基化偶联反应仅在三碘芳烃空间位阻最小的位置引发,这导致了高度的化学选择性转化。在缺电子的1,2,3-三碘芳烃与富电子的苄基酮之间的反应中观察到了最高产率,然而,优化后的反应条件被发现对广泛的不同官能团具有耐受性。这种由1,2,3-三碘苯前所未有的合成7-碘苯并呋喃的方法具有可扩展性、适用范围广,并为其他化学转化提供了获得有价值前体的简便途径。