化学
弗里德尔-克拉夫茨反应
催化作用
路易斯酸
三氟甲磺酸
烷基化
产量(工程)
有机化学
原子经济
溶剂
路易斯酸催化
冶金
材料科学
作者
Sankalan Mondal,Deblina Roy,Manoj K. Jaiswal,Gautam Panda
标识
DOI:10.1016/j.tetlet.2017.11.049
摘要
Using indium (III) triflate as a mild Lewis acid catalyst, the Friedel Crafts alkylation of o-hydroxy bisbenzylic alcohols with aromatic/heteroaromatic arenes under solvent free conditions was achieved to give the corresponding unsymmetrical triarylmethanes in high yields (up to 80% yield). Calculation of the different green metrics for the above reaction revealed it to have high atom economy (94–96%), high reaction mass efficiency (66–77%) and high carbon efficiency (70–80%). The Lewis acid was found to be air and moisture tolerant. The protocol was found to be operationally simple and can be carried out in an “open-flask” leaving behind water as the sole by product. Gratifyingly the Lewis acid catalyst could be recycled and reused up to 5 catalytic cycles without compromising much on the yield thus further highlighting the importance of the protocol.
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