Reaktion #56946
ord-117d740f4ce941b198f1a4abcf68544e
Reaktionsgleichung
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturat reflux under argon for 24 h
- 2EinengenThe suspension was concentrated under reduced pressure
- 3Sonstigethe residue was sonicated with 1M HCl (aq) over 1.5 h
- 4SonstigeThe resultant orange solid was isolated by filtration
- 5Waschenwashed with water
- 6Sonstigedried
- 7Sonstigesonicated with t-butyl methyl ether
- 8Sonstigeisolated by filtration
- 9Sonstigedried
- 10SonstigeWhere necessary, the product was further purified by recrystallisation
Vorschrift
4-Fluoro-3-nitrobenzoic acid (0.27 mol), an aniline (0.32 mol) and NMM (32.5 mL) in 2-methoxyethanol (750 mL) were stirred at reflux under argon for 24 h. The suspension was concentrated under reduced pressure and the residue was sonicated with 1M HCl (aq) over 1.5 h. The resultant orange solid was isolated by filtration, washed with water dried, then sonicated with t-butyl methyl ether, isolated by filtration and dried. Where necessary, the product was further purified by recrystallisation to yield the 4-anilino-3-nitrobenzoic acid: e.g. 4-(3-bromophenyl amino)-3-nitrobenzoic acid. (In some cases, for example with heteroaromatic anilines, NMN may be omitted from the reaction mixture).