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HRID 857873作成日:2026年10月27日

Potassium Carbonate → 2-(2,4-Dimethoxybenzylamino)-4-methylaniline

https://huagongshe.com/reaction/857873

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Ammonium ChlorideHCID 25517—
反応物Benzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
反応物2,3-DimethoxybenzylamineHCID 78106—
触媒IronHCID 23925—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物2-(2,4-Dimethoxybenzylamino)-4-methylanilineHCID 2238572367.1%

反応条件

温度120 °C

反応手順

2,3-Dimethoxybenzylamine (1.05 g) and potassium-carbonate (1.52 g) were added to a solution of 3-fluoro-4-nitrotoluene (0.832 g) in 1-methyl-2-pyrrolidinone (5.0 ml), and the mixture was stirred at 120° C. for 4 hours. Then, ether was added to the reaction mixture. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo to give a yellow oil. The yellow oil was dissolved in ethanol (100 ml), and to the solution were added water (50 ml), saturated aqueous ammonium chloride (50 ml) and iron dust (352 g). The mixture was heated under reflux for 3 hours while vigorous stirring. Then insolubles were removed by filtration, and the filtrate was concentrated in vacuo. The residue was dissolved in chloroform, and the organic layer was washed with water and brine and dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate, 3:1 to 2:1) and then recrystallized by ethyl acetate-hexane to give the title compound (0.980 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07148224B2
出典データセットuspto-grants-2006_12
ORD IDord-3e441a221e094f7184f773fbdac704c8
出典メモuspto-grants-2006_12