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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939314Generated: November 2, 2026

4-(2-methyl-1-(1H)-imidazolyl)-1-phenyl-1-butanone → 4-(2-Methyl-1-(1H)-imidazolyi)-1-phenyl-1-butanone O-(2-aminoethyl)oxime dihydrochloride

https://huagongshe.com/reaction/1939314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-methyl-1-(1H)-imidazolyl)-1-phenyl-1-butanoneHCID 12154158—
Reactant2-(O-aminooxy)ethylamine dihydrochlorideHCID 14362326—
SolventEthanolHCID 702—
Product4-(2-Methyl-1-(1H)-imidazolyi)-1-phenyl-1-butanone O-(2-aminoethyl)oxime dihydrochlorideHCID 86751061109.4%

Reaction Steps

A mixture of 4-(2-methyl-1-(1H)-imidazolyl)-1-phenyl-1-butanone (3.00 g), O-(2-aminoethyl)hydroxylamine dihydrochloride (2.35 g), 3 equivalents of pyddine, and absolute ethanol (75 ml) was heated under reflux, under nitrogen, with stirring, for four hrs. The solvent was evaporated toluene was added and evaporated The residue was partitioned between 10% sodium hydroxide solution and ethyl acetate. The layers were separated and the aqueous phase extracted with ethyl acetate. The combined organic extracts were dried over anhydrous sodium sulfate, filtered, and the filtrate was evaporated. The residue was purified by flash chromatography (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. The precipitate was collected and recrystallized from absolute ethanol/ether to give 3.1 g (66%) of product, mp 153°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696142
Source datasetuspto-grants-1997_12
ORD IDord-627ec51c553c46fa8e4e929b748494cc
Source noteuspto-grants-1997_12