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HRID 228571作成日:2026年10月26日

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

https://huagongshe.com/reaction/228571

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-Chloro-6,7-dimethoxyquinolineHCID 459610—
反応物2-Hydroxy-5-(trifluoromethoxy)benzaldehydeHCID 1268058—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒ChlorobenzeneHCID 7964—
生成物2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehydeHCID 23078303—

反応条件

温度130 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560558B2
出典データセットuspto-grants-2009_07
ORD IDord-cd988899331d4b8587f8382755d24441
出典メモuspto-grants-2009_07