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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828787Generated: October 26, 2026

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

https://huagongshe.com/reaction/1828787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminobenzoic AcidHCID 7419—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant2-Oxo-2-phenylethyl 3-[(trifluoroacetyl)amino]benzoateHCID 1159354—
SolventDichloromethaneHCID 6344—
Product3-[(Trifluoroacetyl)amino]benzoic acidHCID 283840—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060723B2
Source datasetuspto-grants-2006_06
ORD IDord-3fdd3df81f3047e497b4b7ab2b25a666
Source noteuspto-grants-2006_06