Fox Andrew, Ball Liam T
School of Chemistry, University of Nottingham, Nottingham NG7 2RD, U.K.
Org Process Res Dev. 2024 Feb 7;28(2):632-639. doi: 10.1021/acs.oprd.3c00509. eCollection 2024 Feb 16.
The scope and practical utility of bismuth(V)-mediated electrophilic arylation have been greatly improved by the recent development of user-friendly protocols based on modular bismacycle reagents. Here, we report the scalable synthesis of a new bench-stable bismacycle bromide and demonstrate that it can be used as a "universal precursor" in electrophilic arylation. Relative to established syntheses of related bismacycles, the new protocol benefits from improved step- and vessel-economy, reduced production time, and the complete elimination of cryogenic temperatures and undesirable solvents (EtO and CHCl). The synthesis is complemented by a robust, chromatography-free purification procedure that was developed by using design of experiments. We show that this process is highly reproducible at the 100 mmol scale, with two independent experiments giving 61 and 62% yields of isolated material. We anticipate that this efficient method for the synthesis of a new bismacycle precursor will expedite both (a) wider uptake of existing bismuth-mediated arylation methods by the synthetic community and (b) ongoing efforts to develop new bismuth-mediated transformations.
基于模块化双环试剂的用户友好型方案的最新进展,极大地提高了铋(V)介导的亲电芳基化反应的范围和实际效用。在此,我们报告了一种新型易于保存的双环溴化物的可扩展合成方法,并证明它可作为亲电芳基化反应中的“通用前体”。相对于已有的相关双环化合物的合成方法,新方案具有步骤经济性和容器经济性提高、生产时间缩短以及完全无需低温条件和不良溶剂(EtO和CHCl)的优点。该合成方法辅以通过实验设计开发的强大的无需柱色谱的纯化程序。我们表明,此过程在100 mmol规模下具有高度可重复性,两个独立实验得到的分离产物产率分别为61%和62%。我们预计,这种合成新型双环前体的有效方法将加速以下两个方面的进程:(a)合成界对现有铋介导的芳基化方法的更广泛采用;(b)开发新型铋介导转化反应的持续努力。