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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30536생성일: 2026년 10월 24일

Water → (2-(4-Fluorophenoxy)-ethyl)-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/30536

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-FluorophenolHCID 9732—
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl N-(2-((methylsulfonyl)oxy)ethyl)carbamateHCID 22605302—
용매DimethylformamideHCID 6228—
생성물(2-(4-Fluorophenoxy)-ethyl)-carbamic acid tert-butyl esterHCID 2313403657.4%

반응 단계

Next, to a solution of 4-fluorophenol (0.47 g, 4.18 mmol) in DMF (10 mL) was added cesium carbonate (2.72 g, 8.36 mmol) at room temperature. The mixture was stirred at ambient temperature for 15 minutes, then methanesulfonic acid 2-(tert-butoxycarbonylamino)ethyl ester (1.00 g, 4.18 mmol) was added. The reaction mixture was stirred at 100° C. for 16 hours. Water was added and the mixture was concentrated in vacuo. Product mixture was dissolved in ethyl acetate and was washed with water, then with brine. The organic layer was dried over Na2SO4, and the solvent was removed under reduced pressure. The residue was purified by column chromatography (ethyl acetate:hexane=7:1 to 4:1), and obtained [2-(4-fluorophenoxy)ethyl]carbamic acid tert-butyl ester as yellow oil (0.61 g, 57.4% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423175B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-6ea6e05ed63f45a6a9ae7d06ee7857cb
출처 메모uspto-grants-2008_09