Singh Manjit, Prasad Poonam Rajesh
Department of Chemistry, Institute of Science, Banaras Hindu University Varanasi UP 221005 India
RSC Adv. 2025 Jun 18;15(26):20623-20628. doi: 10.1039/d5ra01979f. eCollection 2025 Jun 16.
An efficient C-C cross-coupling approach for the synthesis of α,β-unsaturated ketones was developed through C(sp)-H functionalization of acetophenone and methylarene under thermal conditions in the presence of a green catalyst, FeCl·6HO, with DMF as a solvent and atmospheric O (air) as an oxidant. The method was useful for a wide range of substrates, indicating good functional group compatibility and providing an innovative approach to forming new C-C bonds from inexpensive, readily available starting materials. Thus, the main advantages of the present methods are one-pot reactions, environmentally friendly approaches, cost-effectiveness, broad substrate scope, short reaction times, easy workup procedures, and good yields.
通过在绿色催化剂FeCl·6H₂O存在下,以DMF为溶剂、大气中的O₂(空气)为氧化剂,在热条件下对苯乙酮和甲基芳烃进行C(sp)-H官能化,开发了一种高效合成α,β-不饱和酮的C-C交叉偶联方法。该方法适用于多种底物,显示出良好的官能团兼容性,并提供了一种从廉价、易得的起始原料形成新C-C键的创新方法。因此,本方法的主要优点是一锅反应、环境友好、成本效益高、底物范围广、反应时间短、后处理程序简单且产率高。