On April 30, 2020, Vol’eva, V. B.; Zhorin, V. A.; Ovsyannikova, M. N.; Kurkovskaya, L. N. published an article.Computed Properties of 96-76-4 The title of the article was Solid-Phase ortho-Hydroxylation of 2,4-Di-tert-butylphenol and Its Derivatives. And the article contained the following:
Direct phenol-catechol conversion was realized as a result of the solid-phase reaction of 2,4-di-tert-butylphenol with cuprous oxide under high pressure and shear deformation on the Bridgman anvils. The yield of 3,5-di-tert-butylcatechol in this reaction was about 85%. When cupric oxide was used in the solid-phase process, oxidative coupling of the starting phenol took place, resulting in quant. formation of tetra-tert-butyl-ortho-bisphenol. The reaction of 6-substituted derivatives of 2,4-di-tert-butylphenol with cuprous oxide was used as an example to demonstrate the possibility of substitutive ortho-hydroxylation yielding 7-20% of pyrocatechols. The experimental process involved the reaction of 2,4-Di-tert-butylphenol(cas: 96-76-4).Computed Properties of 96-76-4
The Article related to hydroxy ditertiary butylphenol preparation, ditertiary butylphenol ortho hydroxylation, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Phenols, Thiophenols, and Derivatives Including Phenol and Thiophenol Ethers and Esters and other aspects.Computed Properties of 96-76-4
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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts