A visible-light-mediated trifluoromethylation protocol was developed for the conversion of (hetero)aromatic thiols to their respective S-trifluoromethylated derivatives employing trifluoromethanesulfonyl chloride (CF3SO2Cl) as a cost-effective source of trifluoromethyl radical (CF3·) and a highly reducing organophotocatalyst, 3DPA2FBN. The developed methodology is operationally simple, providing access
开发了一种可见光介导的三
氟甲基化方案,使用三
氟甲
磺酰氯 (CF 3 SO 2 Cl) 作为
三氟甲基自由基 (CF 3 ·) 的经济有效来源,将(杂)芳香族
硫醇转化为其各自的S -三
氟甲基化衍
生物以及高还原性有机光催化剂 3DPA2FBN。所开发的方法操作简单,可以以高达 92% 的收益率获得各种产品。根据初步的机制研究,包括照射开/关、紫外可见光研究和自由基捕获实验,推测了一种合理的机制。