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Effect of Microwave Irradiation on Friedel-Crafts Diphenylmethylation of Arenes

机译:微波辐射对芳烃Friedel-Crafts二苯甲基化的影响

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The reaction between diphenylmethanols and substituted benzenes is useful to yield triarylmethane derivatives which are important skeletons in various functional materials and biologically relevant substances. The Reactions were carried out under microwave irradiation as environmentally-friendly method. In cyclohexane, the reaction was accelerated under microwave irradiation as compared to under conventional heating. Also, when more than 0.8 equivalents of iron(III) chloride were used, the acceleration was observed. Notably, when iron(III) chloride and arenes were combined, the temperature of the reaction solution rose to 40 style="color:#4F4F4F;font-family:" font-size:14px;white-space:normal;background-color:#ffffff;"="">°C. It is considered that a chemical species was formed upon coordination of iron(III) chloride to the diphenylmethanols or arenes.
机译:二苯基甲醇与取代的苯之间的反应可用于产生三芳基甲烷衍生物,该衍生物是各种功能材料和生物学相关物质中的重要骨架。反应在微波辐射下作为环境友好的方法进行。在环己烷中,与常规加热相比,在微波辐射下反应得以加速。另外,当使用大于0.8当量的氯化铁(III)时,观察到加速。值得注意的是,当氯化铁(III)和芳烃结合使用时,反应溶液的温度升至40 style =“ color:#4F4F4F; font-family:” font-size:14px; white-space:normal; background -color:#ffffff;“ =”“>°C。认为化学物种是在氯化铁(III)与二苯甲醇或芳烃配位时形成的。

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