Author:
Hartshorn MP,Ing HT,Richards KE,Sutton KH,Vaughan J
Abstract
The nitrations of the
2-methylphenols (1a) and (1b) give initially 4-nitrocyclohexa-2,5-dienones (6),
which undergo further reaction to yield 2,5-dinitrocyclohex-3-enones (4).
Reactions of these and other related compounds are reported which point towards
a mechanism of formation of substituted 2,5-dinitrocyclohex-3-enones from
2-methylphenols.
Cited by
21 articles.
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