Photoredox/Nickel Dual Catalysis-Enabled Aryl Formylation with 2,2-Dimethoxy- N , N -dimethylethan-1-amine as CO Source.
Jie GaoXian-Chen HeYan-Ling LiuPin-Pin YaoJian-Ping GuanKai ChenHao-Yue XiangJun-An XiaoPublished in: Organic letters (2024)
Herein, a dual photoredox/nickel catalyzed formylation of aryl bromide with commercially available 2,2-dimethoxy- N , N -dimethylethan-1-amine as an effective CO source has been successfully achieved, delivering a series of aromatic aldehydes in moderate to good yields. Compared with the traditional reductive carbonylation process, this newly designed synthetic protocol provides a straightforward toolbox to access aromatic aldehydes, obviating the use of carbon monoxide and stoichiometric reductants. Finally, the utility of this direct formylation reaction was demonstrated in the pharmaceutical analogue synthesis.