Bhattacharya Trisha, Ghosh Animesh, Maiti Debabrata
Department of Chemistry, Indian Institute of Technology Bombay Powai Mumbai Maharashtra 400076 India
Tokyo Tech World Research Hub Initiative (WRHI), Laboratory for Chemistry and Life Science, Tokyo Institute of Technology Tokyo 152-8550 Japan.
Chem Sci. 2021 Feb 10;12(11):3857-3870. doi: 10.1039/d0sc06937j.
Among numerous solvents available for chemical transformations, 1,1,1,3,3,3-hexafluoro-2-propanol (popularly known as HFIP) has attracted enough attention of the scientific community in recent years. Several unique features of HFIP compared to its non-fluoro analogue isopropanol have helped this solvent to make a difference in various subdomains of organic chemistry. One such area is transition metal-catalyzed C-H bond functionalization reactions. While, on one side, HFIP is emerging as a green and sustainable deep eutectic solvent (DES), on the other side, a major proportion of Pd-catalyzed C-H functionalization is heavily relying on this solvent. In particular, for distal aromatic C-H functionalizations, the exceptional impact of HFIP to elevate the yield and selectivity has made this solvent irreplaceable. Recent research studies have also highlighted the H-bond-donating ability of HFIP to enhance the chiral induction in Pd-catalyzed atroposelective C-H activation. This perspective aims to portray different shades of HFIP as a magical solvent in Pd-catalyzed C-H functionalization reactions.
在众多可用于化学转化的溶剂中,1,1,1,3,3,3-六氟-2-丙醇(通常称为HFIP)近年来已引起科学界的充分关注。与非氟类似物异丙醇相比,HFIP的几个独特特性有助于这种溶剂在有机化学的各个子领域中脱颖而出。其中一个领域是过渡金属催化的C-H键官能化反应。一方面,HFIP正成为一种绿色且可持续的深共熔溶剂(DES),另一方面,大部分钯催化的C-H官能化反应严重依赖这种溶剂。特别是对于远端芳族C-H官能化反应,HFIP提高产率和选择性的特殊作用已使这种溶剂不可替代。最近的研究还强调了HFIP的氢键供体能力在钯催化的对映选择性C-H活化中增强手性诱导的作用。本文旨在描绘HFIP作为钯催化的C-H官能化反应中神奇溶剂的不同方面。