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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644243Generated: October 25, 2026

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

https://huagongshe.com/reaction/1644243

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 numberUS08124612B2
Source datasetuspto-grants-2012_02
ORD IDord-304cd3a7fc2741df9afbb97c8fd81e0a
Source noteuspto-grants-2012_02