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3,5-Di-tert-butylcatechol
CAS number: 1020-31-1
3,5-Di-tert-butylcatechol, also known as 3,5-DTBC, is a substituted catechol, meaning it's a benzene ring with two hydroxyl groups (-OH) and two tert-butyl groups (C(CH3)3) attached. It's a crystalline powder, often used as a polymerization inhibitor and stabilizer for monomers like styrene and butadiene.

Related images

Oxidation of the 3,5-di-tert-butylcatechol by the catalyst.
Oxidation of the 3,5-di-tert-butylcatechol by the catalyst.
DOI: /10.1016/j.ica.2011.06.024
Dependence of the reaction rates on pH for the oxidation of 3,5-di-tert-butyl-catechol (3,5-DTBC) catalyzed by 1.
Dependence of the reaction rates on pH for the oxidation of 3,5-di-tert-butyl-catechol (3,5-DTBC) catalyzed by 1.
DOI: /10.1016/j.ica.2011.06.024

Related Questions and Answers

Q: What are the products formed from the oxidation of 3,5-di-tert-butylcatechol and 2-aminophenol by (diacetoxyiodo)benzene?
A: The oxidation of 3,5-di-tert-butylcatechol by (diacetoxyiodo)benzene yields 3,5-di-tert-butylbenzoquinone, while the oxidation of 2-aminophenol results in the formation of 2-amino-3H-phenoxazine-3-one.
Q: What is the role of (diacetoxyiodo)benzene in the oxidation of 3,5-di-tert-butylcatechol and 2-aminophenol?
A: (Diacetoxyiodo)benzene acts as a stoichiometric oxidant, driving the oxidation of 3,5-di-tert-butylcatechol to 3,5-di-tert-butylbenzoquinone and 2-aminophenol to 2-amino-3H-phenoxazine-3-one. The oxidation process involves a radical reaction pathway, and the reactivity of (diacetoxyiodo)benzene is significantly influenced by the solvent medium.