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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366892Generated: October 25, 2026

Ammonium formate → 4-(4-Methyl-1h-imidazol-1-yl)benzenamine

https://huagongshe.com/reaction/2366892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant4-Methyl-1-(4-nitrophenyl)-1H-imidazoleHCID 16005169—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(4-Methyl-1h-imidazol-1-yl)benzenamineHCID 1600517090.5%

Reaction Steps

Ammonium formate (2.202 g, 34.9 mmol) and palladium (10% w/w on carbon, 50% wet, 0.473 g, 4.44 mmol) were added to a solution 4-methyl-1-(4-nitrophenyl)-1H-imidazole (4.73 g, 23.28 mmol) in ethanol (150 mL) and the resulting mixture was refluxed under nitrogen for 1 h then cooled to room temperature. An extra portion of ammonium formate (2.202 g, 34.9 mmol) was then added and the resulting mixture was refluxed for a further hour then cooled to room temperature and filtered through celite. Most of the solvent was removed in vacuo and the residue was loaded on a 50 g SCX column which was eluted with MeOH (5 CV) then with 2N NH3 in MeOH (5 CV). The ammonia fractions were combined and concentrated in vacuo to give 4-(4-methyl-1H-imidazol-1-yl)aniline (3.92 g, 21.06 mmol, 90%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697725B2
Source datasetuspto-grants-2014_04
ORD IDord-132032d583f441b4ae41e7687144151f
Source noteuspto-grants-2014_04