Li Rui, Wu Yongmeng, Wang Changhong, He Meng, Liu Cuibo, Zhang Bin
Department of Chemistry, Institute of Molecular Plus, School of Science, Tianjin University, Tianjin, 300072, China.
Haihe Laboratory of Sustainable Chemical Transformations, Tianjin, 300192, China.
Nat Commun. 2022 Oct 10;13(1):5951. doi: 10.1038/s41467-022-33779-8.
Developing a step-economical approach for efficient synthesis of α,β-deuterio aryl ethylamines (α,β-DAEAs) with high deuterium ratios using an easy-to-handle deuterated source under ambient conditions is highly desirable. Here we report a room-temperature one-pot two-step transformation of aryl acetonitriles to α,β-DAEAs with up to 92% isolated yield and 99% α,β-deuterium ratios using DO as a deuterium source. The process involves a fast α-C - H/C - D exchange and tandem electroreductive deuteration of C ≡ N over an in situ formed low-coordinated Fe nanoparticle cathode. The moderate adsorptions of nitriles/imine intermediates and the promoted formation of active hydrogen (H*) on unsaturated Fe sites facilitate the electroreduction process. In situ Raman confirms co-adsorption of aryl rings and the C ≡ N group on the Fe surface. A proposed H*-addition pathway is confirmed by the detected hydrogen and carbon radicals. Wide substrate scope, parallel synthesis of multiple α,β-DAEAs, and successful preparation of α,β-deuterated Melatonin and Komavine highlight the potential.
开发一种步骤经济的方法,在环境条件下使用易于处理的氘源高效合成具有高氘比的α,β-氘代芳基乙胺(α,β-DAEAs)是非常可取的。在此,我们报道了一种室温下单锅两步法,以DO作为氘源,将芳基乙腈转化为α,β-DAEAs,分离产率高达92%,α,β-氘比高达99%。该过程涉及在原位形成的低配位铁纳米颗粒阴极上快速进行α-C-H/C-D交换和C≡N的串联电还原氘化。腈/亚胺中间体的适度吸附以及不饱和铁位点上活性氢(H*)的促进形成有助于电还原过程。原位拉曼光谱证实了芳环和C≡N基团在铁表面的共吸附。检测到的氢和碳自由基证实了所提出的H*加成途径。广泛的底物范围、多种α,β-DAEAs的平行合成以及α,β-氘代褪黑素和科马文的成功制备突出了其潜力。