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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228590생성일: 2026년 10월 26일

5-Bromo-2-hydroxybenzophenone → {5-Bromo-2-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-(phenyl)methanone

https://huagongshe.com/reaction/228590

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참여 물질

역할이름HCID투입량
반응물5-Bromo-2-hydroxybenzophenoneHCID 229009—
반응물4-Chloro-6,7-dimethoxyquinolineHCID 459610—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매1,2-DichlorobenzeneHCID 7239—
생성물{5-Bromo-2-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-(phenyl)methanoneHCID 2487921094.5%

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온도160 °C

반응 단계

4-Chloro-6,7-dimethoxyquinoline (56.1 mg), 5-bromo-2-hydroxybenzophenone (361 mg), and 4-dimethylaminopyridine (168 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 160° C. for 7 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 mixture was washed with a 1 N aqueous potassium hydroxide solution and saturated brine and was dried over anhydrous magnesium 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 (110 mg, yield 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-6f3beb0d05994b94832df27083e012ea
출처 메모uspto-grants-2009_07