Abstract
Chlorosulfonation of 2-nitroanisole gave 4-methoxy-3- nitrobenzenesulfonyl chloride (7) which was converted with N-butyl(3- phenylpropyl)amine into benzenesulfonamide (8). Hydrolysis of the ether and reduction of the nitro group of 8 followed by diazotization and coupling with 2- naphthol gave N-Butyl-N-(3-phenylpropyl)-4-hydroxy-3-(2-hydroxy- l-naphthyl)azobenzenesulfonamide (1d). © 1993, Taylor & Francis Group, LLC. All rights reserved.
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CITATION STYLE
Katritzky, A. R., Wu, J., Rachwal, S., Macomber, D., & Smith, T. P. (1993). A Novel Method for the Preparation of 3-Amino-4-Hydroxybenzenesulfonamide Precursors of “Acid Alizarin Violet N” Derivatives. Synthetic Communications, 23(3), 405–417. https://doi.org/10.1080/00397919308009795
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