DIPEA-induced activation of OH− for the synthesis of amides via photocatalysis. Issue 23 (16th May 2022)

• Record Type: Journal Article
• Authors: Wu, Mei; Huang, Sheng; Hou, Huiqing; Lin, Jie; Lin, Mei; Zhou, Sunying; Zheng, Zhiqiang; Sun, Weiming; Ke, Fang
• Is Part Of: RSC advances. Volume 12:Issue 23(2022)
• Page Start: 14724
• Page End: 14728
• Publication Date: 2022-05-16
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d2ra02107b
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Under weak organic base condition DIPEA as a reductant to increase the nucleophilicity of H2 O an excellent potential system for nitrile degradation. Abstract : The development of green protocols for photocatalysis where water acts as a nucleophile, induced by a weak organic base, is difficult to achieve in organic chemistry. Herein, an efficient light-mediated strategy for the synthesis of amides in which a weak organic base acts as a reductant to induce the formation of OH– from water under metal-free conditions is reported. A mechanistic study reveals that the generation of an N, N -diisopropylethylamine (DIPEA) radical via single electron transfer (SET), with the assistance of photocatalyst, that increases the nucleophilicity of the water molecules with respect to the cyanides is essential. Moreover, the removal rate of nitrile in wastewater can be as high as 83%, indicating that this strategy has excellent potential for nitrile degradation.