4.6 Article

Direct Amidation from Alcohols and Amines through a Tandem Oxidation Process Catalyzed by Heterogeneous-Polymer-Incarcerated Gold Nanoparticles under Aerobic Conditions

Journal

CHEMISTRY-AN ASIAN JOURNAL
Volume 8, Issue 11, Pages 2614-2626

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.201300733

Keywords

alcohols; amides; heterogeneous catalysis; nanoparticles; oxidation

Funding

  1. Japan Society for the Promotion of Science (JSPS)
  2. Global COE Program
  3. NEDO
  4. University of Tokyo
  5. MEXT, Japan
  6. Japan Science and Technology Agency (JST)
  7. Grants-in-Aid for Scientific Research [24106707, 21225002, 24750035] Funding Source: KAKEN

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We describe herein a highly elegant and suitable synthesis of amide products from alcohols and amines through a tandem oxidation process that uses molecular oxygen as a terminal oxidant. Carbon-black-stabilized polymer-incarcerated gold (PICB-Au) or gold/cobalt (PICB-Au/Co) nanoparticles were employed as an efficient heterogeneous catalyst depending on alcohol reactivity and generated only water as the major co-product of the reaction. A wide scope of substrate applicability was shown with 42 examples. The catalysts could be recovered and reused without loss of activity by using a simple operation.

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