Synlett 2025; 36(20): 3387-3390
DOI: 10.1055/a-2705-8871
Letter

Additive- and Catalyst-free Deoxygenative Reduction of Amides and Imides to Amines with Ammonia Borane

Autoren

  • Ke Xu

    1   School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, P. R. China (Ringgold ID: RIN47862)
    2   Materials Tech Laboratory for Hydrogen & Energy Storage, Ningbo Institute of Materials Technology and Engineering of the Chinese Academy of Sciences, Ningbo, P. R. China (Ringgold ID: RIN74748)
  • Min-Jie Zhou

    1   School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, P. R. China (Ringgold ID: RIN47862)
  • Xinrui Liu

    1   School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, P. R. China (Ringgold ID: RIN47862)
  • Guofei Chen

    3   Laboratory of Polymers and Composites, Ningbo Institute of Materials Technology and Engineering of the Chinese Academy of Sciences, Ningbo, P. R. China (Ringgold ID: RIN74748)
  • Yinjun Xie

    2   Materials Tech Laboratory for Hydrogen & Energy Storage, Ningbo Institute of Materials Technology and Engineering of the Chinese Academy of Sciences, Ningbo, P. R. China (Ringgold ID: RIN74748)

Gefördert durch: Ningbo Natural Science Foundation 2024J114
Gefördert durch: 3315 Program of Ningbo 2020A-32-C
Funding Information This work was supported by the 3315 Program of Ningbo (2020A-32-C), Zhejiang Provincial Natural Science Foundation of China (LQ24B020002), and the Ningbo Natural Science Foundation (2024J114)


Graphical Abstract

Abstract

The reduction of carbonyl compounds is one of the most fundamental and useful transformations in synthetic chemistry. However, due to the high resonance stability of the amide group, reducing amide compounds is difficult and always requires harsh reductants and/or additional catalysts/additives. In this report, we describe a catalyst-free, additive-free protocol for the deoxygenative reduction of amides using ammonia borane as a mild reductant. Tertiary, secondary, and primary amides, as well as challenging imides can be reduced to the corresponding amines under these conditions. Additionally, the transformation performed well in open air, making the method more practical.



Publikationsverlauf

Eingereicht: 20. Juni 2025

Angenommen nach Revision: 01. September 2025

Accepted Manuscript online:
19. September 2025

Artikel online veröffentlicht:
24. Oktober 2025

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