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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 990439생성일: 2026년 10월 24일

4-Fluorophenol → 1-(4-Fluorophenoxy)-3-nitrobenzene

https://huagongshe.com/ko/reaction/990439

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorophenolHCID 9732—
반응물1,2-DinitrobenzeneHCID 10707—
반응물Cesium carbonateHCID 10796—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물1-(4-Fluorophenoxy)-3-nitrobenzeneHCID 2350603072%

반응 조건

온도100 °C

반응 단계

EX-634A) Dinitrobenzene (1.68 g, 10 mmol) and 4-fluorophenol (1.13 g, 10 mmol) were dissolved in anhydrous dimethylsulfoxide (25 mL), and powdered cesium carbonate (8 g, 24.8 mmol) was added. The mixture was stirred and heated to 100° C. using a reflux condenser under a nitrogen atmosphere. After 16 h, the mixture was diluted with water (120 mL), and the aqueous layer was extracted with diethyl ether (4×60 mL). The combined ether layers were washed with 3% HCl, 5% sodium hydroxide, and water, then dried over anhydrous MgSO4. The ether was removed in vacuo, and the recovered oil was purified by flash column chromatography on silica gel eluting with ethyl acetate in hexane (1:25) to give 1.68 g (69%) of the desired 3-(4-fluorophenoxy)nitrobenzene product as orange crystals, 97% pure by HPLC analysis. MS m/z=234 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06458803B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-080868011fc847dd8875a2b64ca02354
출처 메모uspto-grants-2002_10