Reactions of benzazole-2-thiones with 3,5-di-tert-butyl-4-hydroxybenzyl acetate

The benzylation of benzothiazole(oxazole, imidazole)-2-thiones with 3,5-di- tert -butyl-4-hydroxybenzyl acetate involves either the sulfur or nitrogen atom depending on the reaction conditions. The S - and N -benzylation products of benzazole-2-thiones are kinetically and thermodynamically controlle...

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Veröffentlicht in:Russian journal of general chemistry 2017, Vol.87 (1), p.22-28
Hauptverfasser: Tagasheva, R. G., Gataullina, D. R., Zaripova, I. F., Bukharov, S. V., Nugumanova, G. N., Deberdeev, T. R., Voronina, Yu. K.
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Sprache:eng
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Zusammenfassung:The benzylation of benzothiazole(oxazole, imidazole)-2-thiones with 3,5-di- tert -butyl-4-hydroxybenzyl acetate involves either the sulfur or nitrogen atom depending on the reaction conditions. The S - and N -benzylation products of benzazole-2-thiones are kinetically and thermodynamically controlled products, respectively. The use of 3,5-di- tert -butyl-4-hydroxy-benzyl acetate allows sterically hindered hydroxybenzyl derivatives of benzаzole-2-thiones to be generally synthesized under milder conditions than in known methods of their synthesis.
ISSN:1070-3632
1608-3350
DOI:10.1134/S1070363217010054