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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604863Generated: October 25, 2026

1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazole → 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline

https://huagongshe.com/reaction/604863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazoleHCID 45480180—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 4548018178.3%

Reaction Steps

2520 mg (10.8 mmol) 1-(2-methoxy-4-nitro-phenyl)-4-methyl-1H-imidazole dissolved in ethanol (110 ml) was hydrated under an atmosphere of hydrogen at room temperature for 3½ hours in the presence of 252 mg of 10% palladium on charcoal. The catalyst was filtered off and washed with ethanol. The solvent of the filtrate was evaporated under reduced pressure. The crude product was purified on silica gel with methylene chloride/methanol 19/1. The fraction containing the product was suspended in diethyl ether, stirred for 15 minutes, filtered and dried to yield 1719 mg (78%) 3-methoxy-4-(4-methyl-imidazol-1-yl)-phenylamine as a yellow solid. MS ISP (m/e): 204.3 (100) (M+H)+. 1H NMR (CDCl3, 250 MHz): δ (ppm)=7.48 (s, 1H), 6.91 (d, 1H), 6.88 (s, 1H), 6.35 (s, 1H), 6.17 (d, 1H), 3.68 (s, 3H), 2.11 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910740B2
Source datasetuspto-grants-2011_03
ORD IDord-cdfdc24091ba44b497bd55592611929c
Source noteuspto-grants-2011_03