Abstract
The addition of thioacetic acid to 2,6-di-tert-butyl-4-(phosphorylmethylidene)cyclohexa-2,5-dien-1-ones has been accomplished for the first time. The resulting adduct is readily hydrolyzed with hydrazine hydrate to give 2,6-di-tert-butyl-4-[phosphoryl(sulfanyl)methyl]phenols, and the latter reacted with the initial quinomethanes, yielding 4,4′-[sulfanediylbis(phosphorylmethylene)]bis(2,6-di-tert-butylphenols).
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Dedicated to B.I. Buzykin on the 80th Anniversary of His Birth
Original Russian Text © M.B. Gazizov, R.K. Ismagilov, A.L. Pistsova, N.S. Tikhonova, L.P. Shamsutdinova, R.N. Burangulova, R.F. Karimova, 2017, published in Zhurnal Obshchei Khimii, 2017, Vol. 87, No. 12, pp. 2080–2083.
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Gazizov, M.B., Ismagilov, R.K., Pistsova, A.L. et al. Synthesis and Properties of Some Sulfur-Containing Derivatives of Phosphorylated Sterically Hindered Phenols. Russ J Gen Chem 87, 2891–2894 (2017). https://doi.org/10.1134/S1070363217120246
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DOI: https://doi.org/10.1134/S1070363217120246