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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21519생성일: 2026년 10월 25일

Ethyl Acetate → Methyl {p-{5-[(2-chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-2-nitroanilino}phenoxy}acetate

https://huagongshe.com/reaction/21519

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물Methyl(4-aminophenoxy)acetateHCID 6422115—
반응물2-Chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl 3-fluoro-4-nitrophenyl etherHCID 86748717—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물Methyl {p-{5-[(2-chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-2-nitroanilino}phenoxy}acetateHCID 8674871619.4%

반응 조건

온도80 °C

반응 단계

A mixture of 2-chloro-α,α,α,6-tetrafluoro-p-tolyl 3-fluoro-4-nitrophenyl ether (2.1 g, 0.006 mol), methyl (p-aminophenoxy)acetate (2.7 g, 0.015 mol) and potassium carbonate (2.0 g, 0,015 mol) in N,N-dimethyl formamide is stirred at 80° C. for 18 hours, cooled to room temperature, poured into brine and extracted with ethyl acetate. The organic extract is washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain a residue. Flash chromatography of the residue using silica gel and a 20% ethyl acetate in hexanes solution gives the title product as a red oil (0.6 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-83e80843e5f64dcf9c75d52225a97513
출처 메모uspto-grants-1995_06