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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1644243생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1644243

반응식

참여 물질

역할이름HCID투입량
반응물3-Aminobenzoic AcidHCID 7419—
반응물Trifluoroacetic anhydrideHCID 9845—
반응물2-Oxo-2-phenylethyl 3-[(trifluoroacetyl)amino]benzoateHCID 1159354—
용매DichloromethaneHCID 6344—
생성물3-[(Trifluoroacetyl)amino]benzoic acidHCID 283840—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124612B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-304cd3a7fc2741df9afbb97c8fd81e0a
출처 메모uspto-grants-2012_02