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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34487Generated: October 27, 2026

Imidazole → 1-(2,4-Dichlorophenyl)-3-(imidazol-1-yl)-2-phenylpropan-1-one

https://huagongshe.com/reaction/34487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant1-(2,4-Dichlorophenyl)-2-phenylpropen-1-oneHCID 129438—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(2,4-Dichlorophenyl)-3-(imidazol-1-yl)-2-phenylpropan-1-oneHCID 13749942—

Reaction Steps

A solution of 1-(2,4-dichlorophenyl)-2-phenylpropen-1-one (4g), imidazol (1.36 g) and tetramethylquanidine (0.5 ml) in tetrahydrofuran (100 ml) was heated at reflux for 12 hours. The reaction mixture was cooled and concentrated under reduced pressure to yield a gum. The gum was dissolved in ethyl acetate, washed with distilled water, and acidified with 4N hydrochloric acid. The aqueous phase was basified with sodium carbonate and extracted with ethyl acetate. The organic phase was separated, washed with distilled water, dried over anhydrous magnesium sulphate and concentrated under reduced pressure to yield an oil which was chromatographed on silica gel using a mixture of methanol/dichloromethane (1:9) as an eluent to yield 1-(2,4-dichlorophenyl)-3-(imidazol-1-yl)-2-phenylpropan-1-one (600 mg), which was treated with ethereal hydrogen chloride to yield the hydrochloride salt of 1-(2,4-dichlorophenyl)-3-(imidazol-1-yl)-2-phenylpropan-1-one, m.p. 110° C., (Found: C, 55.38; H, 4.37; N, 7.40%; C18H15Cl3N2O.1/2H2O requires C, 55.34; H, 4.13; N, 7.17%) having the formula: ##STR28##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761483
Source datasetuspto-grants-1988_08
ORD IDord-991c45a866e3470fb33e38814f1b128a
Source noteuspto-grants-1988_08