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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28668Erstellt: 23. Oktober 2026

Aniline → 4-Anilino-3-nitrobenzoic acid

https://huagongshe.com/de/reaction/28668

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnilineHCID 6115—
Edukt4-MethylmorpholineHCID 7972—
Edukt4-Fluoro-3-nitrobenzoic acidHCID 67987—
Lösungsmittel2-MethoxyethanolHCID 8019—
Produkt4-Anilino-3-nitrobenzoic acidHCID 3824366—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419995B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-117d740f4ce941b198f1a4abcf68544e
Quellennotizuspto-grants-2008_09