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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857873Generated: October 25, 2026

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

https://huagongshe.com/reaction/857873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
Reactant2,3-DimethoxybenzylamineHCID 78106—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-(2,4-Dimethoxybenzylamino)-4-methylanilineHCID 2238572367.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148224B2
Source datasetuspto-grants-2006_12
ORD IDord-3e441a221e094f7184f773fbdac704c8
Source noteuspto-grants-2006_12