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HRID 14505생성일: 2026년 10월 25일

Ammonia → 2-(4-Chlorophenyl)-1-(4-fluoro-2-hydroxy-phenyl)-ethanone

https://huagongshe.com/reaction/14505

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물3-FluorophenolHCID 9743—
반응물4-Chlorophenylacetyl chlorideHCID 90692—
반응물Aluminum(III) ChlorideHCID 6451240—
용매1,2-DichloroethaneHCID 11—
용매DichloromethaneHCID 6344—
생성물2-(4-Chlorophenyl)-1-(4-fluoro-2-hydroxy-phenyl)-ethanoneHCID 68702520—

반응 조건

온도0 °C

반응 단계

To a solution of 4-chlorophenylacetyl chloride (27.6 g, 0.15 mol) in 1,2-dichloroethane (200 ml), cooled to 0° C. in an ice bath, under nitrogen is added slowly AlCl3 (21.8 g, 0.16 mol). The reaction mixture is stirred at 0° C. for 20 min. 3-fluorophenol (12.2 g, 0.11 mol) is added, and the reaction mixture is allowed to warm to room temperature, then heated at 90° C. for 16 h. The reaction mixture is cooled to room temperature, then poured cautiously into aqueous ammonia solution (500 ml) with vigourous stirring. The mixture is diluted with CH2Cl2 (250 ml) and filtered through Celite. The organic phase is separated, washed with water, brine and dried (MgSO4). The solvent is removed in vacuo, and the crude product is purified by flash chromatography on silica gel using iso-hexane:ethyl acetate (10:1 to 4:1) as the eluent to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732435B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-44e1dcc8469d4abfa6010145fe0f0cf5
출처 메모uspto-grants-2010_06