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Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

reactions of 2-t-Butyl-4,6-dimethylphenol, 2,4-Di-t-butyl-6-methylphenol and 2,4,6-Tri-t-butylphenol with Nitrogen Dioxide

MP Hartshorn, WT Robinson, KH Sutton and J Vaughan

Australian Journal of Chemistry 38(1) 161 - 177
Published: 1985

Abstract

Reaction of 2-t-butyl-4,6-dimethylphenol(10) with nitrogen dioxide in benzene gives the C4-epimeric 4,5,6-trinitrocyclohex-2-enones (13) and (14). In contrast, similar reaction of 2,4-di-t-butyl-6-methyl-phenol (11) gives substituted cyclohex-3-enones, 2,5,6-trinitro ketones (20)- (23), 2-hydroxy-5,6-dinitro ketones (27) and (28) and the 6-hydroxy- 2,5-dinitro ketone (29). Reaction of 2,4,6-tri-t-butylphenol (12) with nitrogen dioxide gives initially the 4-nitro dienone (35), but de-t- butylated products (36) and (37) are formed in long-term reactions. X- ray crystal structures are reported for compounds (13),(14),(21),(22), (23), (27), (28) and (29).

https://doi.org/10.1071/CH9850161

© CSIRO 1985

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