Faculty of Pharmacy, UMR 8076, BioCIS, Univ. Paris-Sud, CNRS , University Paris-Saclay , 92290 Châtenay-Malabry , France.
J Org Chem. 2018 Nov 16;83(22):14001-14009. doi: 10.1021/acs.joc.8b02361. Epub 2018 Nov 7.
We report here a method of direct Friedel-Crafts benzylation of arenes with benzylic alcohols using cheap and readily available bisulfate salt as the catalyst in hexafluoroisopropanol. The catalytic system is powerful with a quite diverse group of functionalized arenes and benzylic alcohols. These mild conditions provide a straightforward synthesis of a variety of unsymmetrical diarylmethanes in high yield with good to high regioselectivity. An S1 mechanism involving activation of the hydroxy group through a hydrogen bond is proposed.
我们在此报告了一种使用廉价易得的硫酸盐盐作为催化剂,在六氟异丙醇中直接进行芳基与苄醇的 Friedel-Crafts 苄基化反应的方法。该催化体系对功能化芳基和苄醇具有很强的催化作用。在温和的条件下,以高区域选择性和良好的收率得到了多种不对称二芳基甲烷的直接合成。提出了一种 S1 反应机理,其中通过氢键活化羟基。