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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21510생성일: 2026년 10월 25일

Water → 4-[(2-Chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-2-(p-methoxyphenoxy)-1-nitrobenzene

https://huagongshe.com/reaction/21510

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-MethoxyphenolHCID 9015—
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl 3,4-dinitrophenyl etherHCID 86748711—
용매AcetonitrileHCID 6342—
생성물4-[(2-Chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-2-(p-methoxyphenoxy)-1-nitrobenzeneHCID 8674871225.2%

반응 단계

A mixture of 2-chloro-α,α,α,6-tetrafluoro-p-tolyl 3,4-dinitrophenyl ether (10.0 g, 0.026 mol), 4methoxyphenol (6.45 g, 0.052 mol) and potassium carbonate (7.26 g, 0.052 mol) in acetonitrile is refluxed for 18 hours, cooled to room temperature, poured into water and extracted with ethyl acetate. The organic extract is washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain an amber oil. Column chromatography of the oil using silica gel and a (1:4) ether/hexanes solution gives the title product as a yellow oil (3.0 g) which is identified by 1HNMR and 13CNMR spectral analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424280
출처 데이터셋uspto-grants-1995_06
ORD IDord-e3ab984d5c024708ae7185b42301c498
출처 메모uspto-grants-1995_06