Department of Chemistry, Indian Institute of Technology Ropar, Lab no. 406, S. S. Bhatnagar Block, Rupnagar, Punjab 140001, India.
Org Lett. 2022 Apr 1;24(12):2310-2314. doi: 10.1021/acs.orglett.2c00439. Epub 2022 Mar 21.
The synthesis of paracetamol still relies on multistep protocols involving the utilization of a stoichiometric amount of oxidizing/reducing or other corrosive agents. Herein we report a regioselective electrochemical Ritter-type reaction at the C(sp)-H of unprotected phenol toward the environmentally benign and direct synthesis of paracetamol. The reaction proceeds under exogenous oxidant- and catalyst-free conditions. The protocol is scalable, can be deployed to a variety of phenols, and offers a sustainable alternative for the synthesis of paracetamol.
对乙酰氨基酚的合成仍然依赖于多步反应方案,其中涉及使用化学计量的氧化剂/还原剂或其他腐蚀性试剂。在此,我们报告了一种在未保护的苯酚的 C(sp)-H 位置上进行的区域选择性电化学 Ritter 型反应,该反应是一种环境友好且直接合成对乙酰氨基酚的方法。该反应在外源氧化剂和催化剂不存在的条件下进行。该方案具有可扩展性,可应用于多种苯酚,并为对乙酰氨基酚的合成提供了一种可持续的替代方法。