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Synlett 2015; 26(16): 2288-2292
DOI: 10.1055/s-0034-1381060
DOI: 10.1055/s-0034-1381060
letter
One-Step Synthesis of Nitriles from Acids, Esters and Amides Using DIBAL-H and Ammonium Chloride
Further Information
Publication History
Received: 11 June 2015
Accepted after revision: 09 August 2015
Publication Date:
03 September 2015 (online)


Abstract
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.
Key words
nitrile - carboxylic acid - diisobutylaluminum hydride - aluminum amide - ammonium chlorideSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0034-1381060.
- Supporting Information