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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904650Generated: October 30, 2026

Imidazole → 1-(2,4-Dichlorophenoxy)-3,3-dimethyl-4-fluoro-1-(imidazol-1-yl)-2-butanone hydrochloride

https://huagongshe.com/reaction/904650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant1-Bromo-1-(2,4-dichlorophenoxy)-3,3-dimethyl-4-fluoro-2-butanoneHCID 13019444—
SolventAcetonitrileHCID 6342—
Product1-(2,4-Dichlorophenoxy)-3,3-dimethyl-4-fluoro-1-(imidazol-1-yl)-2-butanone hydrochlorideHCID 2047850578.6%

Reaction Steps

157.5 g (0.44 mol) of 1-bromo-1-(2,4-dichlorophenoxy)-3,3-dimethyl-4-fluoro-2-butanone were dissolved in 500 ml of acetonitrile and the solution was added dropwise to a solution of 109 g (1.6 mol) of imidazole in 600 ml of acetonitrile. The mixture was heated under reflux for 10 hours. Thereafter, the solvent was distilled off under a waterpump vacuum, the residue was taken up in 1,000 ml of methylene chloride and the methylene chloride mixture was washed three times with 500 ml of water each time. The organic phase was dried over sodium sulphate, filtered and concentrated under a waterpump vacuum by distilling off the solvent. The residue was dissolved in 500 ml of ethanol, 40 ml each of concentrated hydrochloric acid were added and the solvent was distilled off under a waterpump vacuum. The residue was stirred with 500 ml of ether, whereupon it crystallized. 66 g (39.3% of theory) of 1-(2,4-dichloro-phenoxy)-3,3-dimethyl-4-fluoro-1-(imidazol-1 -yl)-2-butanone hydrochloride of melting point 91°-110° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04419361
Source datasetuspto-grants-1983_12
ORD IDord-7d7b93fdfbb948a0aad5980bae385c27
Source noteuspto-grants-1983_12