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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 521822생성일: 2026년 10월 25일

Water → 4-Cyclopropyl-2-fluoro-1-nitrobenzene

https://huagongshe.com/reaction/521822

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DichloromethaneHCID 6344—
반응물Cesium carbonateHCID 10796—
반응물Cyclopropylboronic acidHCID 2760897—
반응물3-Fluoro-4-nitrophenyl trifluoromethanesulfonateHCID 21998735—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매TolueneHCID 1140—
생성물4-Cyclopropyl-2-fluoro-1-nitrobenzeneHCID 5742391491.7%

반응 조건

온도90 °C

반응 단계

A mixture of 3-fluoro-4-nitrophenyl trifluoromethanesulfonate (7.15 g, 24.73 mmol), cyclopropylboronic acid (2.55 g, 29.67 mmol), [1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II), complexed with dichloromethane (1:1) (1.62 g, 1.98 mmol), and 2M cesium carbonate in water (19.8 mL, 39.56 mmol) in toluene (39.5 mL) was degassed for 20 min. The reaction mixture was stirred at 90° C. under N2 for 2.5 h. The reaction was cooled to RT, diluted with ethyl acetate (200 mL), and filtered through a pad of Celite. The filtrate was washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude residue was purified via flash column chromatography eluted with 0 to 75% DCM/hexane to give 4.11 g (91.7%) of 4-cyclopropyl-2-fluoro-1-nitrobenzene as an oil. 1H NMR (400 MHz, MeOD) δ 7.98 (dd, J=10.2, 6.6 Hz, 1H), 7.12-7.02 (m, 2H), 2.11-1.97 (m, 1H), 1.20-1.11 (m, 2H), 0.89-0.82 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328106B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-70c988a1222b4ebaa89d61ae43e69663
출처 메모uspto-grants-2016_05