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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128486생성일: 2026년 10월 23일

Water → 5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide

https://huagongshe.com/ko/reaction/128486

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
반응물N,N-diethyl-5-fluoro-2-nitrobenzamideHCID 12999068—
용매Dimethyl SulfoxideHCID 679—
용매Benzene hexaneHCID 110624—
생성물5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamideHCID 1533501981.6%

반응 단계

To a 100 ml flask fitted with a magnetic stirrer and drying tube is added dimethyl sulfoxide (30 ml), anhydrous potassium carbonate (7.55 g, 0.054 mole) and 2-chloro-4-trifluoromethylphenol (10.3 g, 0.052 mole). The mixture is stirred at room temperature overnight. A solution of N,N-diethyl-5-fluoro-2-nitrobenzamide (12.5 g, 0.052 mole) in dimethyl sulfoxide (20 ml) is then added rapidly and the reaction mixture is stirred at room temperature for 60 hours. The reaction mixture is poured into water (500 ml) and the product extracted into carbon tetrachloride (4×100 ml), the combined extracts are dried over anhydrous magnesium sulfate and the solvent removed under vacuum to afford 15.3 g of 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide (75% yield) Recrystallization from benzene/hexane affords substantially pure product mp. 75°-79° C. Elemental anal, Calcd. for C18H16ClF3N2O4 : C, 51.80; H, 3.88; Cl, 8.55; F, 13.68; N, 6.73. Found: C, 52.03; H, 3.90; Cl, 8.54; F, 13.59; N, 6.83.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04259510
출처 데이터셋uspto-grants-1981_03
ORD IDord-58e228bb23604395be2422d3b310d73b
출처 메모uspto-grants-1981_03