Abstract
Alkyl splitting of 4-acetylamino-N-(3,5-di-tert-butyl-4-hydroxybenzyl)benzenesulfonamide with alkali solution has been discovered, the reaction being uncommon for amides. The driving force of the process is the tendency of 3,5-di-tert-butyl-4-hydroxybenzyl derivatives to eliminate 2,6-di-tert-butyl-4-methylenecyclohexa-2,5-dienone in the presence of bases.
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Original Russian Text © Yu.N. Oludina, E.D. Ibatullina, S.V. Bukharov, G.N. Nugumanova, R.G. Tagasheva, R.Ya. Deberdeev, 2015, published in Zhurnal Obshchei Khimii, 2015, Vol. 85, No. 2, pp. 209–212.
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Oludina, Y.N., Ibatullina, E.D., Bukharov, S.V. et al. Reaction of alkyl splitting of 4-acetylamino-N-(3,5-di-tert-butyl-4-hydroxybenzyl)-benzenesulfonamide. Russ J Gen Chem 85, 383–386 (2015). https://doi.org/10.1134/S1070363215020061
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DOI: https://doi.org/10.1134/S1070363215020061