- Reduction of aromatic nitro compounds with hydrogen gas over a platinum catalyst gives anilines. A variation is formation of a dimethylaminoarene with palladium on carbon and formaldehyde:[5]
- The Leimgruber-Batcho, Bartoli and Baeyer-Emmerling indole syntheses begin with aromatic nitro compounds.
- Indigo can be synthesized in a condensation reaction from ortho-nitrobenzaldehyde and acetone in strongly basic conditions in a reaction known as the Baeyer-Drewson indigo synthesis[6]
- The presence of nitro groups facilitates nucleophilic aromatic substitution because they are very electron-withdrawing.
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