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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378899Generated: October 23, 2026

4-Methoxybenzenecarboximidamide → 2-(4-Methoxyphenyl)-4-(2-nitrophenyl)imidazole

https://huagongshe.com/en/reaction/378899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzenecarboximidamideHCID 229074—
Reactant2-Bromo-2'-nitroacetophenoneHCID 244025—
SolventAcetonitrileHCID 6342—
Product2-(4-Methoxyphenyl)-4-(2-nitrophenyl)imidazoleHCID 17848892378.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 2-bromo-2′-nitroacetophenone (18 g), 4-methoxybenzamidine (20 g), and silica gel (20 g) in acetonitrile (500 ml) is heated at 40° C. for 24 hours. The reaction is evaporated and the residue put on a layer of silica gel and eluted with 50% ethyl acetate/hexane (1500 ml). The solution is evaporated under reduced pressure to approximately 250 ml and extracted with 5% HCl (3×250 ml). The combined aqueous solution is basified with K2CO3 and extracted with ethyl acetate (3×400 ml) to afford 2-(4-methoxyphenyl)-4-(2-nitrophenyl)-imidazole (17 g) as a dark yellow oil which is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297252B1
Source datasetuspto-grants-2001_10
ORD IDord-ad59b6e86cc441af88a72d2c9740d441
Source noteuspto-grants-2001_10