A novel two-step synthesis of isonitrosoacetanilides [2-(hydroxyimino)-N-phenylacetamides] has been developed, involving the initial acylation of aniline derivatives with 2,2-diacetoxyacetyl chloride, followed by reaction with hydroxylamine hydrochloride. The method works equally well with a variety of different aniline derivatives, including those with poor aqueous solubility and those containing electron rich ortho-substituents, neither of which react well under traditional conditions. (c) 2005 Elsevier Ltd. All rights reserved.
Martinet; Coisset, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1921, vol. 172, p. 1235
作者:Martinet、Coisset
DOI:——
日期:——
Martinet; Caisset, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1921, vol. 172, p. 1234
作者:Martinet、Caisset
DOI:——
日期:——
Sandmeyer, Helvetica Chimica Acta, 1919, vol. 2, p. 239
作者:Sandmeyer
DOI:——
日期:——
An improved synthesis of isonitrosoacetanilides
作者:Gordon W. Rewcastle、Hamish S. Sutherland、Claudette A. Weir、Adrian G. Blackburn、William A. Denny
DOI:10.1016/j.tetlet.2005.10.046
日期:2005.12
A novel two-step synthesis of isonitrosoacetanilides [2-(hydroxyimino)-N-phenylacetamides] has been developed, involving the initial acylation of aniline derivatives with 2,2-diacetoxyacetyl chloride, followed by reaction with hydroxylamine hydrochloride. The method works equally well with a variety of different aniline derivatives, including those with poor aqueous solubility and those containing electron rich ortho-substituents, neither of which react well under traditional conditions. (c) 2005 Elsevier Ltd. All rights reserved.