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HRID 1828787作成日:2026年10月26日

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

https://huagongshe.com/reaction/1828787

反応式

関与物質

役割名称HCID仕込み量
反応物3-Aminobenzoic AcidHCID 7419—
反応物Trifluoroacetic anhydrideHCID 9845—
反応物2-Oxo-2-phenylethyl 3-[(trifluoroacetyl)amino]benzoateHCID 1159354—
溶媒DichloromethaneHCID 6344—
生成物3-[(Trifluoroacetyl)amino]benzoic acidHCID 283840—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07060723B2
出典データセットuspto-grants-2006_06
ORD IDord-3fdd3df81f3047e497b4b7ab2b25a666
出典メモuspto-grants-2006_06