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A one-step base-free synthesis of N -arylamides via modified pivaloyl mixed anhydride mediated amide coupling.

Fenghua MaoCan JinJie WangHui YangXinhuan YanXiaoqing LiXiangsheng Xu
Published in: Organic & biomolecular chemistry (2023)
Pivalic anhydride is shown to be an effective reagent for direct amidation of carboxylic acids with N -alkyl anilines. The only by-product of this reaction is nontoxic pivalic acid, which can be easily removed by aqueous workup. The reactions are conducted under mild conditions and found to be compatible with a range of carboxylic acids, including aromatic, heterocyclic, acrylic, and aliphatic carboxylic acids and amino acids generating the desired amides in short reaction times.
Keyphrases
  • amino acid
  • ionic liquid
  • room temperature
  • electron transfer