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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17673생성일: 2026년 10월 24일

Water → 1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene

https://huagongshe.com/ko/reaction/17673

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물p-FluoronitrobenzeneHCID 9590—
반응물Potassium CarbonateHCID 11430—
반응물4-Fluoro-3-(trifluoromethyl)phenolHCID 601854—
용매DimethylformamideHCID 6228—
생성물1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzeneHCID 66977640—

반응 조건

온도90 °C

반응 단계

To a stirred solution of 4-fluoronitrobenzene (20 mmol), 4-fluoro-3-trifluoromethylphenol (22 mmol) in DMF (50 mL) at rt, solid potassium carbonate (60 mmol) was added, and the reaction mixture was heated to 90° C. for 5 h (monitored by TLC), according to General Procedure L1. After cooling to rt, the reaction mixture was poured into cold H2O (60 mL). The resulting mixture was extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with H2O (2×40 mL) and brine (50 mL), and dried over anhydrous sodium sulfate. The solvent was removed in vacuuo to afford the desired 1-fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene. The crude product was used directly for further transformation without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737285B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9fa8fdd3cb6347bd92ef71732b136c84
출처 메모uspto-grants-2010_06