Metal-Free C−S Bond Cleavage

  • ChemPubSoc Europe Logo
  • Author: European Journal of Organic Chemistry
  • Published Date: 11 September 2019
  • Source / Publisher: European Journal of Organic Chemistry/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
thumbnail image: Metal-Free C−S Bond Cleavage

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The activation and transformations of C–S bonds in thioether compounds is useful, e.g., in the petroleum industry and in organic chemistry. Such reactions usually rely on the insertion of a transition-metal catalyst into the C−S bond, leading to C−S bond cleavage.


Ke Yang, Yi Li, Zhiyan Ma, Long Tang, Yue Yin, Hao Zhang, Zhengyi Li and Xiaoqiang Sun, Changzhou University, China, have developed an efficient metal-free C−S bond cleavage process. The method allows the team to access different  β-aminopropanamide and acrylamide derivatives. Using Selectfluor as an "F+" reagent, a variety of N-substituted acrylamides were synthesized from N-substituted 3-methylthiopropanamides in 1,4‐dioxane (reaction pictured). The products were obtained in good to excellent yields.


The reaction can also be used to convert the thioethers to amine derivatives: When different N-substituted 3-methylthiopropanamides were reacted with amines in the presence of Selectfluor, N-substituted β-aminopropanamides were obtained in moderate to good yields.


Mechanistic investigations indicate that the N-substituted 3-methylthiopropanamides are converted the corresponding thionium intermediates or sulfoxides in the presence of Selectfluor, both of which can then be further transformed into N-substituted acrylamides and β-aminopropanamides.


 

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