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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228571생성일: 2026년 10월 25일

Water → 2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehyde

https://huagongshe.com/reaction/228571

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-Chloro-6,7-dimethoxyquinolineHCID 459610—
반응물2-Hydroxy-5-(trifluoromethoxy)benzaldehydeHCID 1268058—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매ChlorobenzeneHCID 7964—
생성물2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehydeHCID 23078303—

반응 조건

온도130 °C

반응 단계

4-Chloro-6,7-dimethoxyquinoline (111 mg), 5-trifluoromethoxysalicylaldehyde (412 mg), and 4-dimethylaminopyridine (244 mg) were suspended in monochlorobenzene (2 ml), and the suspension was stirred at 130° C. overnight. The reaction solution was cooled to room temperature, water was then added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water 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 chromatography on silica gel using ethyl acetate-hexane for development to give 2-[(6,7-dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehyde.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-cd988899331d4b8587f8382755d24441
출처 메모uspto-grants-2009_07