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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325987Generated: October 30, 2026

Hydrochloric Acid → (1Z)-1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanone oxime

https://huagongshe.com/reaction/325987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHydroxylamine HClHCID 21645—
Reactant1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethan-1-oneHCID 32232—
SolventMethanolHCID 887—
Product(1Z)-1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanone oximeHCID 5480616—

Reaction Steps

1240 g (4.9 moles) of the thus prepared 2,4-dichlorophenacyl-1H-imidazol is dissolved in 6.2 l methanol. 506.6 g (7.3 moles) hydroxylammonium chloride and 818.2 g KOH (14.6 moles) are added to this solution, which then is heated for one hour under reflux while stirring. After cooling the reaction mixture is poured into 5330 ml aqueous HCl having a concentration of 5% by weight, whereby the oxime product is precipitated. About one hour later the solid product is filtered off and well washed with water. Then after well drying the thus obtained raw product is recrystallized from ethylene glycol monomethyl ether. The pure oxime product, i.e. the (Z)-1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)-ethanone oxime thus is obtained in the form of colourless crystals having a melting point of 227°-229° C. The yield is 89%. The purity and the identity of the obtained product were confirmed by chemical analysis, TLC, NMR and IR absorption spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443612
Source datasetuspto-grants-1984_04
ORD IDord-8d8c95a3eae940c1ade67d1b843b7e3f
Source noteuspto-grants-1984_04