Visible-Light-Mediated Three-Component Decarboxylative Coupling Reactions to Synthesize 1,4-Diol Monoethers

• Published in: Journal of organic chemistry Vol. 88; no. 19; pp. 13871 - 13882
• Main Authors: Wang, Ai, Yin, Yu-Yun, Rukhsana, Wang, Le-Quan, Jin, Jia-Hui, Shen, Yong-Miao
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 06.10.2023; Amer Chemical Soc
• Subjects: Chemistry; Chemistry, Organic; Physical Sciences; Science & Technology; ACYL CHLORIDES; PHOTOREDOX; AMINO-ACIDS; CASCADE; ELECTRON-DEFICIENT ALKENES; DICARBOFUNCTIONALIZATION; ALKYLATIONS; RADICAL-ADDITION; DUAL CATALYSIS; CARBOXYLIC-ACIDS
• ISSN: 0022-3263; 1520-6904
• DOI: 10.1021/acs.joc.3c01483

An efficient approach for 1,2-difunctionalization of aromatic olefins and the synthesis of functionalized 1,4-diols monoethers has been established via a photoinduced three-component reaction of an α-alkoxycarboxylic acid, an aromatic olefin, and an aldehyde. The reaction proceeds by photoinduced oxidative decarboxylation of the carboxylic acid followed by the addition of the α-alkoxyalkyl radical to the olefin, one-electron reduction of the addition radical, and the nucleophilic attack of the resulting carbanion to the aldehyde. Besides the convenient one-pot protocol of the three-component reaction, this method offers several other advantages, including good functional group tolerance for the three substrates, gentle reaction conditions, and ease of scaling up. The reaction mechanism has been investigated through free radical trapping experiment and isotope labeling experiments.