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New Opportunities for Duff Reaction
Authors:I S Belostotskaya  N L Komissarova  T I Prokof’eva  L N Kurkovskaya  V B Vol’eva
Institution:(1) Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, Moscow, 119991, Russia
Abstract:Reaction of 2,4-di-tert-butylphenol with urotropin in conditions of Duff reaction takes an abnormal route and instead of the expected di-tert-butylsalicylaldehyde provides a mixture of N-substituted 3,5-di-tert-butyl-2-hydroxybenzylamines and redox conjugate benzoxazines containing mostly 6,8-di-tert-butyl-3-(3,5-di-tert-butyl-2-hydroxybenzyl)-2H-3,4-dihydrobenze]1,3]oxazine. A solvolysis of an individual benzoxazine in the system HO(CH2)2OH-H2O-HCl affords di(3,5-di-tert-butyl-2-hydroxybenzyl)amine, and in AcOH 3,5-di-tert-butylsalicilaldehyde. A mechanism of Duff reaction was suggested involving the formation of a benzoxazine intermediate.__________Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 5, 2005, pp. 718–721.Original Russian Text Copyright © 2005 by Belostotskaya, Komissarova, Prokof’eva, Kurkovskaya, Vol’eva.
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