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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1296173생성일: 2026년 10월 26일

4-Fluoro-3-nitrobenzoic acid → 4-Fluoro-3-nitro-N,N-bis(2,2,2-trifluoroethyl)benzamide

https://huagongshe.com/reaction/1296173

반응식

참여 물질

역할이름HCID투입량
반응물4-Fluoro-3-nitrobenzoic acidHCID 67987—
반응물Bis(2,2,2-trifluoroethyl)amineHCID 78999—
반응물DiisopropylethylamineHCID 81531—
반응물DCM thionyl chlorideHCID 21879677—
용매DichloromethaneHCID 6344—
생성물4-Fluoro-3-nitro-N,N-bis(2,2,2-trifluoroethyl)benzamideHCID 58911744—

반응 단계

4-Fluoro-3-nitrobenzoic acid (2.50 g, 13.5 mmol) was refluxed in a 2:1 mixture of CH2Cl2/SOCl2 (150 mL) for 5 h. The solvent was concentrated and the residue was dissolved in CH2Cl2 (50 mL). Another CH2Cl2 solution (50 mL) of diisopropylethylamine (DIPEA) (3.50 mL, 20.3 mmol) and bis(2,2,2-trifluoroethyl)amine (4.90 g, 27.0 mmol) was then added dropwise to the cold stirring solution (0° C.) of the acid chloride. The solution was stirred at rt overnight. The solution was then washed with 5% KHSO4 solution, saturated NaHCO3 solution, brine and dried over anhydrous MgSO4. The crude product was purified by flash chromatography using 3:1/hexanes:EtOAc to afford the title product. Yield: 3.08 g (66%). 1H NMR (400 MHz, CDCl3) δ 4.17 (brs, 4H), 7.40 (t, J=8.59 Hz, 1H), 7.66 (m, 2H), 8.10 (d, J=6.84 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07244850B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-7ef732435ffc410794416f0089413b14
출처 메모uspto-grants-2007_07