Abstract:
Reaction of 3-hydroxy-2,5-di-tert-butyl-1,4-benzoquinone with phenylhydrazine hydrochloride mainly leads to the corresponding hydrazone at the position 1 existing in tautomeric equilibrium with 3,6-di-tert-butyl-4-(phenyl- diazenyl)catechol. Thermodynamic parameters of the tautomerization were evaluated by NMR spectroscopy. The hydrazone structure was confirmed by XRD study.
Citation:
K. A. Martyanov, A. A. Tsybushkina, A. V. Cherkasov, A. A. Belikov, V. A. Kuropatov, “4-Phenyldiazenyl-substituted 3,6-di-tert-butylcatechol: synthesis and azo–hydrazone equilibrium”, Mendeleev Commun., 34:4 (2024), 584–586
Linking options:
https://www.mathnet.ru/eng/mendc195
https://www.mathnet.ru/eng/mendc/v34/i4/p584
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