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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939312Generated: November 2, 2026

Ethanol → 3-(1-(1H)-Imidazolyl)-1-(3-trifluoromethylphenyl)-1-propanone O-(2-aminoethyl)oxime dihydrochloride

https://huagongshe.com/reaction/1939312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPyridineHCID 1049—
Reactant2-(O-aminooxy)ethylamine dihydrochlorideHCID 14362326—
Reactant3-(1-(1H)-imidazolyl)-1-(3-trifluoromethylphenyl)-1-propanoneHCID 19078331—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
Product3-(1-(1H)-Imidazolyl)-1-(3-trifluoromethylphenyl)-1-propanone O-(2-aminoethyl)oxime dihydrochlorideHCID 8675105953.5%

Reaction Steps

A mixture of 3-(1-(1H)-imidazolyl)-1-(3-trifluoromethylphenyl)-1-propanone (4.60 g), O-(2-aminoethyl)hydroxylamine dihydrochloride (3.07 g), 3 equivalents of pyridine, and absolute ethanol (75 ml) was stirred under reflux, under nitrogen, for three hrs. The reaction mixture was diluted with 10% sodium hydroxide solution and ethyl acetate. The layers were separated. The aqueous phase was extracted with ethyl acetate, the organic layers were dried over anhydrous sodium sulfate, filtered, and the filtrate was evaporated. The residue was taken up in toluene and evaporated. The residue was flash chromatographed (180:19:1 dichloromethane/methanol/ammonium hydroxide). The appropriate fractions were collected and concentrated. The residue was dissolved in absolute ethanol and treated with ethereal hydrogen chloride. Diethyl ether was added to the solution. The solid was collected and recrystallized twice from absolute ethanol/ether to give 2.2 g (32%) of product, mp 223°-225° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696142
Source datasetuspto-grants-1997_12
ORD IDord-14bfa3b61c80470994872685e89a5700
Source noteuspto-grants-1997_12