2002
DOI: 10.1039/b207276a
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Disproportionation, isomerization and de-tert-butylation of 2,6-di-tert-butylphenol catalyzed by H-MCM-41

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Cited by 4 publications
(2 citation statements)
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“…This retardation of the rate of reaction suggests the formation of tert-butanol in the oxidation reaction rather than isobutylene (Scheme II/III). Further isobutylene is not expected to be a final product in the present case as it has reported to be found as a byproduct when the reaction is carried out at temperatures of 100 0 C or above [25].…”
Section: (E) Effect Of Tert-butanol On the Oxidation Reactionmentioning
confidence: 70%
“…This retardation of the rate of reaction suggests the formation of tert-butanol in the oxidation reaction rather than isobutylene (Scheme II/III). Further isobutylene is not expected to be a final product in the present case as it has reported to be found as a byproduct when the reaction is carried out at temperatures of 100 0 C or above [25].…”
Section: (E) Effect Of Tert-butanol On the Oxidation Reactionmentioning
confidence: 70%
“…These alkylphenols can be converted to value-added products. For example, alkylphenols are used intensively in the polymer industry as antioxidants, UV absorbers and thermal stabilizers [34]. 2-Ethylphenol and 3-ethylphenol are the starting materials for photochemicals while 4ethylphenol is employed to obtain 4-vinylphenol, an intermediate in the synthesis of pharmaceuticals, dyes, and various antioxidants used in the manufacture of rubbers and polymers [35].…”
Section: Introductionmentioning
confidence: 99%