4.4 Article

One-Step Synthesis of Nitriles from Acids, Esters and Amides Using DIBAL-H and Ammonium Chloride

Journal

SYNLETT
Volume 26, Issue 16, Pages 2288-2292

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1381060

Keywords

nitrile; carboxylic acid; diisobutylaluminum hydride; aluminum amide; ammonium chloride

Funding

  1. University of Bialystok [BST-124]
  2. EU as a part Operational Program Development of Eastern Poland [POPW.01.03.00-20-034/09-00]

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A convenient, one-step procedure is presented for the conversion of carboxylic acids or their derivatives (esters, lactones, amides) to nitriles with an aminoalane reagent prepared from diisobutylaluminum hydride (DIBAL-H) and ammonium chloride.

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