N. A. Magdalinova, T. G. Volkova, M. V. Klyuev
Jun 6, 2010
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Journal
Russian Journal of Organic Chemistry
Abstract
The propanal hydroamination was studied. It was found that the reaction in ethanol proceeded faster than in 2-propanol. By 1H and 13C NMR method the existence was proved of a tautomeric equilibrium in ethanol solution between 4-(propylideneamino)benzoic acid and its enamine form, 4-(prop-1-en-1-ylamino)benzoic acid.