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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1828787Erstellt: 25. Oktober 2026

3-Aminobenzoic Acid → 3-[(Trifluoroacetyl)amino]benzoic acid

https://huagongshe.com/reaction/1828787

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Aminobenzoic AcidHCID 7419—
EduktTrifluoroacetic anhydrideHCID 9845—
Edukt2-Oxo-2-phenylethyl 3-[(trifluoroacetyl)amino]benzoateHCID 1159354—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-[(Trifluoroacetyl)amino]benzoic acidHCID 283840—

Reaktionsschritte

A compound having general Formula 4, exemplified by 3-(2,2,2-Trifluoro-acetylamino)-benzoic acid 2-oxo-2-phenyl-ethyl ester (Compound 4; FIG. 1) can be prepared as follows. A solution of 3-aminobenzoic acid (137 mg, 1.0 mmol) in dichloromethane is treated with trifluoroacetic anhydride (420 mg, 2.0 mmol). The reaction mixture is stirred until no further reaction occurs. The reaction mixture is concentrated to give 3-(2,2,2-Trifluoro-acetylamino)-benzoic acid. A solution of 3-(2,2,2-Trifluoro-acetylamino)-benzoic acid (233 mg, 1.0 mmol) and 2-hydroxyacetophenone (136 mg, 1.0 mmol) in dimethylformamide and diisopropylethylamine (260 mg, 2.0 mmol) is treated with HBTU (379 mg, 1.0 mmol). The reaction mixture is stirred until no further reaction occurs. The reaction is poured into ethyl acetate and water. The organic phase is collected, dried and concentrated to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07060723B2
Quelldatensatzuspto-grants-2006_06
ORD IDord-3fdd3df81f3047e497b4b7ab2b25a666
Quellennotizuspto-grants-2006_06