首页> 外文期刊>Research on Chemical Intermediates >A new efficient method for the preparation of intermediate aromatic ketones by Friedel-Crafts acylation
【24h】

A new efficient method for the preparation of intermediate aromatic ketones by Friedel-Crafts acylation

机译:通过Friedel-Crafts酰化制备中间芳香酮的新高效方法

获取原文
获取原文并翻译 | 示例
           

摘要

As the most important method to prepare pharmaceutical and chemical intermediate aromatic ketones, Friedel-Crafts (F-C) acylation is used to seek a novel catalytic system which is imminently consistent with the concept of green chemistry. In this study, six deep eutectic solvents (DES) were synthesized for the Friedel-Crafts acylation reaction as a catalytic solvent. Among the six DES, choline chloride-zinc chloride ([ChCl][ZnCl2](2)) proved to be the most competent candidate of electron-rich arenes with acylation reagent. It got the highest yield when 1.0 equivalent of [ChCl][ZnCl2](2) used with acyl halides at 70 degrees C. Recycled DES was reused directly without any extra process. After five cycles, the catalytic activity did not decrease significantly (80-85%). Finally, according to experimental validation, the possible mechanism of this reaction was considered.
机译:作为制备药物和化学中间芳族酮的最重要方法,Friedel-Crafts(F-C)酰化用于寻求一种新型催化系统,其与绿色化学的概念一致。 在该研究中,为Friedel-Crafts酰化反应合成了六个深浓度溶剂作为催化溶剂。 在六个DES中,氯化胆碱 - 氯化锌([CHCl] [ZnCl2](2))被证明是富酰化试剂的富含电子的最称重的候选者。 当在70摄氏度下与酰卤相似的[CHCl] [ZnCl2](2)时,在70℃下使用的[CHCl] [ZnCl2](2)时,得到的最高产量。再循环DES直接重复使用而无需任何额外的方法。 经过五个循环后,催化活性没有显着降低(80-85%)。 最后,根据实验验证,考虑了该反应的可能机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号