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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228542생성일: 2026년 10월 26일

2-Acetyl-4-fluorophenol → 1-{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-fluorophenyl}-1-ethanone

https://huagongshe.com/reaction/228542

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참여 물질

역할이름HCID투입량
반응물2-Acetyl-4-fluorophenolHCID 95992—
반응물4-Chloro-6,7-dimethoxyquinolineHCID 459610—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매1,2-DichlorobenzeneHCID 7239—
생성물1-{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-fluorophenyl}-1-ethanoneHCID 2487910172%

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온도160 °C

반응 단계

4-Chloro-6,7-dimethoxyquinoline (58.2 mg), 5-fluoro-2-hydroxyacetophenone (409 mg), and 4-dimethylaminopyridine (317 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 160° C. for 8 hr. The reaction solution was cooled to room temperature, and the solvent was then removed therefrom by distillation under the reduced pressure. Chloroform was added to the residue, and the organic layer was washed with a 1 N aqueous potassium hydroxide solution and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using chloroform and by thin layer chromatography using acetone-hexane to give the title compound (63.5 mg, yield 72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-292ee15e054a4432bd8fe045a6d76269
출처 메모uspto-grants-2009_07