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Continuous Flow Synthesis of N -Sulfonyl-1,2,3-triazoles for Tandem Relay Cu/Rh Dual Catalysis.

Yong-Ju KwonSang-Gi LeeWon-Suk Kim
Published in: The Journal of organic chemistry (2023)
The continuous flow synthesis of N -sulfonyl-1,2,3-triazoles, which are convenient reactive azavinyl carbene precursors, for tandem relay Cu/Rh dual catalysis has been developed. Most reactions readily proceeded at 75 °C in a short residence time of 13.09 min in the presence of 2.5 mol % of CuTC. The scope of the reactions was explored by synthesizing diversely functionalized N -sulfonyl and sulfamoyl triazoles in yields ranging from 92 to 98%. To demonstrate the scalability of the process, the reaction was conducted on a 5.4 mmol scale with residence and collection times of 13.09 and 60 min, respectively. Furthermore, a series of controlled experiments were performed to investigate the compatibility of Cu and Rh in a batch or a continuous flow system. Finally, the first integrated flow system using the azavinyl carbene intermediate under the tandem relay Cu/Rh dual catalysis was developed for the synthesis of various cis -diamino enones from alkynes and sulfonyl azides.
Keyphrases
  • aqueous solution
  • metal organic framework
  • visible light
  • mass spectrometry