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HRID 228687作成日:2026年10月25日

4-Chloro-6,7-dimethoxyquinoline → 4-(2-Iodo-4,5-dimethyl-phenoxy)-6,7-dimethoxyquinoline

https://huagongshe.com/reaction/228687

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-6,7-dimethoxyquinolineHCID 459610—
反応物2-Iodo-4,5-dimethylphenolHCID 13635257—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物4-(2-Iodo-4,5-dimethyl-phenoxy)-6,7-dimethoxyquinolineHCID 2307836157.6%

反応条件

温度130 °C

反応手順

2-Iodo-4,5-dimethylphenol (447 mg), 4-chloro-6,7-dimethoxyquinoline (466 mg), and 4-dimethylaminopyridine (539 mg) were suspended in o-dichlorobenzene (20 ml), and the mixture was stirred at 130° C. for 4 hr. The reaction solution was cooled to room temperature, and the solvent was then removed by distillation under the reduced pressure. Water was then added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography using acetone-chloroform to give the title compound (452 mg, yield 50%).

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-375447432ad448ada733883bacae3148
出典メモuspto-grants-2009_07