Teli Yaqoob A, Reetu Reetu, Chanu S Aleena, Kant Kamal, Keremane Kavya S, Almeer Rafa, Singh Virender, Malakar Chandi C
Department of Chemistry, National Institute of Technology Manipur, Imphal, 795004, India.
Materials Research Institute, The Pennsylvania State University, University Park, PA, 16802, United States.
Chem Asian J. 2024 Nov 4;19(21):e202400635. doi: 10.1002/asia.202400635. Epub 2024 Oct 3.
The distinct roles of different chemical species are essential for the discovery of novel chemical transformations in organic synthesis. Here, we have designed a potential strategy for the synthesis of triarylmethanes (TRAMs) using the dual C(aryl)-alkylation process. This protocol was influenced by 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) as a pivotal reagent and proceeds through the selective para C-H functionalization method. The described approach has been proven to be highly efficient in terms of substrate scope with excellent functional group tolerance and gram scale synthesis of the desired product with 90 % yield. The recyclability and reusability of HFIP has enhanced the feasibility of this protocol towards the sustainable synthesis of TRAMs.
不同化学物种的独特作用对于有机合成中新型化学转化的发现至关重要。在此,我们设计了一种利用双C(芳基)-烷基化过程合成三芳基甲烷(TRAMs)的潜在策略。该方案受1,1,1,3,3,3-六氟异丙醇(HFIP)作为关键试剂的影响,并通过选择性对位C-H官能化方法进行。所描述的方法在底物范围方面已被证明是高效的,具有出色的官能团耐受性,并且能够以90%的产率进行克级规模合成所需产物。HFIP的可回收性和可重复使用性提高了该方案用于TRAMs可持续合成的可行性。