Abstract
The oxidation of 2,6-di-tert-butyl-4-methylphenol with hydrogen peroxide in the presence of potassium iodide gave 3,3′,5,5′-tetra-tert-butyl-4,4′-stilbenequinone which catalyzed liquid-phase oxidation of sodium sulfide with oxygen more efficiently than did 3,3′,5,5′-tetra-tert-butyl-4,4′-diphenoquinone.
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Original Russian Text © H.Y. Hoang, R.M. Akhmadullin, F.Yu. Akhmadullina, R.K. Zakirov, A.G. Akhmadullina, A.S. Gazizov, 2018, published in Zhurnal Organicheskoi Khimii, 2018, Vol. 54, No. 7, pp. 1006–1010.
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Hoang, H.Y., Akhmadullin, R.M., Akhmadullina, F.Y. et al. Synthesis of 3,3′,5,5′-Tetra-tert-butyl-4,4′-stilbenequinone and Its Catalytic Activity in the Liquid-Phase Oxidation of Inorganic Sulfides. Russ J Org Chem 54, 1008–1013 (2018). https://doi.org/10.1134/S1070428018070060
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DOI: https://doi.org/10.1134/S1070428018070060