Kushwaha Ambuj Kumar, Maury Suresh Kumar, Kamal Arsala, Singh Himanshu Kumar, Pandey Shikha, Singh Sundaram
Department of Chemistry, Indian Institute of Technology (BHU), Varanasi - 221 005, UP, India.
Chem Commun (Camb). 2023 Mar 30;59(27):4075-4078. doi: 10.1039/d2cc07001d.
An efficient C-N cross-coupling approach for the synthesis of hydrazones was developed through C(sp)-H and C(sp)-H functionalization of indole and methylarene under visible light irradiation using photocatalyst eosin Y, ethanol:water as a green solvent and atmospheric air as an oxidant. With the aid of eosin Y, the C-H bonds of indole and methylarenes were activated followed by coupling with arylhydrazines. The procedure was applied to a wide variety of substrates with good functional group compatibility, offering a creative way to make hydrazones from inexpensive and easily accessible raw materials. The absence of metals, low cost, environmental friendliness, green solvent, non-toxicity, ease of handling, and utilization of renewable energy sources like visible light are some of this method's primary advantages.
通过使用光催化剂曙红Y、乙醇:水作为绿色溶剂以及大气空气作为氧化剂,在可见光照射下对吲哚和甲基芳烃进行C(sp)-H和C(sp)-H官能化反应,开发了一种高效的用于合成腙的C-N交叉偶联方法。在曙红Y的辅助下,吲哚和甲基芳烃的C-H键被活化,随后与芳基肼偶联。该方法适用于多种具有良好官能团兼容性的底物,为从廉价且易于获得的原料制备腙提供了一种创新方法。该方法的主要优点包括无金属、低成本、环境友好、绿色溶剂、无毒、易于操作以及利用可见光等可再生能源。