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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509559Generated: November 1, 2026

Aniline → methyl 5-(4-methoxybutyl)-2-methyl-1-phenyl-1H-imidazole-4-carboxylate

https://huagongshe.com/reaction/1509559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl 2-(acetylamino)-7-methoxy-3-oxoheptanoateHCID 58355553—
SolventButyronitrileHCID 8008—
Productmethyl 5-(4-methoxybutyl)-2-methyl-1-phenyl-1H-imidazole-4-carboxylateHCID 58355289—

Reaction Steps

Methyl 2-(acetylamino)-7-methoxy-3-oxoheptanoate (5.45 g), aniline (3.01 ml) and trifluoroacetic acid (2.48 ml) were dissolved in butyronitrile (30 ml), and the reaction mixture was heated under reflux for 2 hr. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. 3.6M Aqueous potassium carbonate solution was added to the obtained residue and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (10:90-100:0) was concentrated under reduced pressure to give the object product (3.88 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221836B2
Source datasetuspto-grants-2015_12
ORD IDord-83f47a957bb141dbb6f36f4f5c777da9
Source noteuspto-grants-2015_12