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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53324생성일: 2026년 10월 24일

4-Fluorophenol → 1,3-Dibromo-5-(4-fluorophenoxy)benzene

https://huagongshe.com/ko/reaction/53324

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorophenolHCID 9732—
반응물1,3,5-TribromobenzeneHCID 12279—
반응물Sodium hydrideHCID 24758—
반응물HCID 178418361HCID 178418361—
용매2,4,6-TrimethylpyridineHCID 7953—
생성물1,3-Dibromo-5-(4-fluorophenoxy)benzeneHCID 1996240832.5%

반응 단계

Sodium hydride (3.24 g of 60% suspension in mineral oil was added portionwise to a stirred mixture of 1,3,5-tribromobenzene (76.4 g), 4-fluorophenol (18.16 g), and cuprous oxide (11.6 g) in collidine (400 ml) at room temperature. When evolution of hydrogen had ceased the mixture was heated under reflux with stirring for 8 hours. It was then cooled and filtered. The residue was washed with ethyl acetate followed by concentrated aqueous ammonia, and the combined filtrate and washings were partitioned between ethyl acetate and water. The organic layer was washed twice with brine and evaporated. The residue was dissolved in ethyl acetate, and the solution was filtered, washed several times with citric acid solution and dried (MgSO4). The solvent was evaporated, and the residue was dissolved in hot hexane. The solution was filtered and the filtrate was evaporated. The residue was chromatographed on silica using hexane as eluent to give the title compound as an oil (18.21 g), Rf 0.31(SS 2). Found: C,41.71; H,1.97. C12H7Br2FO requires C,41.66; H,2.04%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618941
출처 데이터셋uspto-grants-1997_04
ORD IDord-32300b7feb6546f497fbc93c293e789c
출처 메모uspto-grants-1997_04