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HRID 228538作成日:2026年10月26日

Water → 2-[(6,7-Dimethoxy-4-quinolyl)oxy]naphthalene-1-carbaldehyde

https://huagongshe.com/reaction/228538

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-Hydroxy-1-naphthaldehydeHCID 12819—
反応物4-Chloro-6,7-dimethoxyquinolineHCID 459610—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物2-[(6,7-Dimethoxy-4-quinolyl)oxy]naphthalene-1-carbaldehydeHCID 2307848215%

反応条件

温度160 °C

反応手順

4-Chloro-6,7-dimethoxyquinoline (100 mg), 2-hydroxy-1-naphthoaldehyde (231 mg), and 4-dimethylaminopyridine (164 mg) were suspended in o-dichlorobenzene (6 ml), and the suspension was stirred at 160° C. for 2 hr. 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 column chromatography using acetone-chloroform to give the title compound (24 mg, yield 15%).

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-3eda3425b3e0483e83bac2f7ede96c50
出典メモuspto-grants-2009_07