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- Indirekte Diazotierung (nach Reduktion der NO2-Gruppe mit Zn/HCl) danach Azo-Kupplung- Vitali-Morin-Reaktion - Zimmermann-Reaktion (nur bis zum Meisenheimer-Salz) (Nw aktivierte Methylengruppen) nach Deprotonierung, nucleophile Substitution der aktiv. Methylengruppe an Dinitrobenzol - Aktivierung mit SOCl2, dann Reaktion mit Hydroxylamin zu Hydroxamsäure —> Komplexbildung mit Fe(III)Cl3 zu rotem Chelatkomplex
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