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通过六氟异丙醇活化催化剂实现缺电子芳烃的协同傅克烷基化反应

Cooperative Friedel-Crafts Alkylation of Electron-Deficient Arenes via Catalyst Activation with Hexafluoroisopropanol.

作者信息

Singh Sanjay, Mondal Sankalan, Tiwari Vikas, Karmakar Tarak, Hazra Chinmoy Kumar

机构信息

Department of Chemistry, Indian Institute of Technology Delhi Hauz Khas, New Delhi, 110016, India.

出版信息

Chemistry. 2023 Mar 28;29(18):e202300180. doi: 10.1002/chem.202300180. Epub 2023 Feb 24.

Abstract

A Friedel-Crafts alkylation of electron-deficient arenes with aldehydes through ''catalyst activation'' is presented. Through hydrogen bonding interactions, the solvent 1,1,1,3,3,3, -hexafluoroisopropanol (HFIP) interacted with the added Brønsted acid catalyst pTSA•H O, increasing its acidity. This activated catalyst enabled the Friedel-Crafts alkylation of electron-neutral as well as electron-deficient arenes. Strongly electron withdrawing arenes including arenes with multiple halogen atoms, NO , CHO, CO R, and CN, groups acted as efficient nucleophiles in this reaction. DFT studies reveal multiple roles of solvent HFIP viz; increasing the Brønsted acidity of the catalyst pTSA•H O, and stabilization of the transition states through a concerted pathway enabling the challenging reaction.

摘要

本文介绍了通过“催化剂活化”实现缺电子芳烃与醛的傅克烷基化反应。通过氢键相互作用,溶剂1,1,1,3,3,3-六氟异丙醇(HFIP)与添加的布朗斯特酸催化剂对甲苯磺酸一水合物(pTSA•H₂O)相互作用,提高了其酸度。这种活化的催化剂能够实现电子中性以及缺电子芳烃的傅克烷基化反应。强吸电子芳烃,包括含有多个卤素原子、NO₂、CHO、COR和CN基团的芳烃,在该反应中作为有效的亲核试剂。密度泛函理论(DFT)研究揭示了溶剂HFIP的多种作用,即提高催化剂pTSA•H₂O的布朗斯特酸度,并通过协同途径稳定过渡态,从而实现这一具有挑战性的反应。

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