A Facile Approach to Catalyst-Free Cyanation and Azidation of ­Organic Compounds and a One-Pot Preparation of 5-Substituted 1H-Tetrazoles by Using a Dimethyl Sulfoxide–Nitric Acid Combination

AuthorsMohammad ali Nasseri,Boshra Mahmoudi,
JournalSynlett
Page number2290-2294
Serial number30
Volume number20
IF2.419
Paper TypeFull Paper
Published At2019
Journal GradeISI
Journal TypeTypographic
Journal CountryBelgium
Journal IndexJCR،Scopus

Abstract

In this study, cyanations or azidations of imines were performed by using hydroxy(dimethyl)-λ4-sulfanecarbonitrile or azido(dimethyl)-λ4-sulfanol, respectively, prepared in situ by treatment of potassium cyanide or sodium azide with a dimethyl sulfoxide–nitric acid combination. Furthermore, a one-pot preparation of 5-substituted 1H-tetrazole derivatives was carried out by using this reagent combination in the presence of an aldehyde, hydroxylamine hydrochloride, and sodium azide under mild conditions.

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tags: dimethyl sulfoxide - nitric acid - Strecker reaction - amino nitriles - amino azides - tetrazoles