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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 229248생성일: 2026년 10월 24일

2-Fluoroanisole → 4-(3-Fluoro-4-methoxy-benzoyl)-benzoic acid methyl ester

https://huagongshe.com/ko/reaction/229248

반응식

참여 물질

역할이름HCID투입량
반응물2-FluoroanisoleHCID 67576—
반응물Methyl 4-(chlorocarbonyl)benzoateHCID 81850—
반응물Aluminum(III) ChlorideHCID 6451240—
용매DichloromethaneHCID 6344—
생성물4-(3-Fluoro-4-methoxy-benzoyl)-benzoic acid methyl esterHCID 6865454717.2%

반응 단계

To an ice-cooled slurry of AlCl3 (2.01 g, 15.1 mmol) in dichloromethane (10 mL) was slowly added 4-chlorocarbonyl-benzoic acid methyl ester (2 g, 10.1 mmol) in dichloromethane (5 mL). The reaction mixture was stirred for 20 min in the ice bath then 2-fluoroanisole (1.4 mL, 12.1 mmol) in dichloromethane (5 mL) was added. The reaction mixture was stirred at room temperature for 20 h. The reaction mixture was poured into ice cold 1 N HCl (10 mL) and the mixture was stirred for 15 min. The reaction mixture was transferred to a separatory funnel and the layers were separated. The aqueous layer was extracted with dichloromethane and the organic extracts were combined, washed with brine, dried over Na2SO4, filtered and concentrated. The crude solid was triturated with hot hexanes, filtered and washed with hexanes to give 0.5 g (17%) of compound 173 as a white powder. 1H NMR (400 MHz, DMSO-d6): δ 3.89 (s, 3H), 3.94 (s, 3H), 7.32 (t, J=8.5 Hz, 1H), 7.57 (d, J=8.8 Hz, 1H), 7.59-7.63 (m, 1H), 7.81 (d, J=8.2 Hz, 2H), 8.04 (s, 1H), 8.10 (d, J=8.3 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560589B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-b64d8e49f5674c098f2dbc283974b5ee
출처 메모uspto-grants-2009_07