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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 857873생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/857873

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Ammonium ChlorideHCID 25517—
반응물Benzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
반응물2,3-DimethoxybenzylamineHCID 78106—
촉매IronHCID 23925—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-(2,4-Dimethoxybenzylamino)-4-methylanilineHCID 2238572367.1%

반응 조건

온도120 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07148224B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-3e441a221e094f7184f773fbdac704c8
출처 메모uspto-grants-2006_12