Keywords
o-quinones
alkylation
electrochemistry
oxidation
phenol
selenium dioxide
tetralines
X-ray study
Abstract
New tri-tert-alkyl substituted o-quinones of 3-tert-alkyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-1,2-dione chemotype were obtained from phenol and 2,5-dichloro-2,5-dimethylhexane, with the SeO2 oxidation of the sterically hindered phenol moiety having been performed at the final step. The electrochemical reduction of these quinones proceeds in two stages: the first reduction wave (E1/2 = –0.60 ÷ –0.62 V) is reversible, while the second stage is irreversible.
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