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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239620생성일: 2026년 10월 26일

Phenylacetic Acid → 1-(5-Fluoro-2-hydroxyphenyl)-2-phenylethanone

https://huagongshe.com/reaction/239620

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참여 물질

역할이름HCID투입량
반응물Phenylacetic AcidHCID 999—
반응물4-FluoroanisoleHCID 9987—
반응물Oxalyl chlorideHCID 65578—
반응물Aluminum(III) ChlorideHCID 6451240—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물1-(5-Fluoro-2-hydroxyphenyl)-2-phenylethanoneHCID 277858556%

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온도0 °C

반응 단계

Phenylacetic acid (8.09 g, 59.46 mmoles) was dissolved in 15 ml dichloromethane. To this mixture, oxalylchloride (5.2 ml, 59.46 mmoles) and DMF (3 drops) were added at 0° C. and stirred for 30 min. The solvent was evaporated and dissolved in 15 ml dichloromethane. To this mixture, 4-fluoroanisole (5.0 g, 39.64 mmoles) was added and cooled to 0° C. At 0° C. AlCl3 (7.92 g, 59.46 mmoles) was added and the reaction mixture was warmed to RT and stirred for 12 h. The reaction mixture was quenched by the addition of 2N HCl, extracted with ethyl acetate, dried over sodium sulphate and concentrated. The crude product was purified by column chromatography with ethyl acetate: petroleum ether to afford the title compound as off-white solid (5.1 g, 56% yield. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 11.43(s,1H), 7.77(dd, J=9.5,3.2 Hz, 1H), 7.42(dt, J=8.7,3.2 Hz, 1H),7.33(t, J=7.3 Hz, 2H), 7.26(m, 3H), 7.01(q, J=4.6 Hz, 1H),4.42(s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642607B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-b76c0f78a5ef4c369bea9509007d13db
출처 메모uspto-grants-2014_02