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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467060Generated: October 26, 2026

Water → 4-(4-Chlorophenyl)-1-(imidazol-1-yl)butan-2-one

https://huagongshe.com/reaction/467060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(4-chlorophenyl)-1-(1H-imidazol-1-yl)-2-butanolHCID 10955994—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product4-(4-Chlorophenyl)-1-(imidazol-1-yl)butan-2-oneHCID 1101033592.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of oxalyl chloride (74.8 g) in dry dichloromethane (1350 mL) at below -70° C. under a nitrogen atmosphere was treated with dry dimethyl sulfoxide (91.5 mL) in methylene chloride (270 mL) dropwise over 15 to 20 minutes while maintaining the temperature of the reaction mixture below -50° C. After an additional 5 minutes a solution of (±)-1-(4-(4-chlorophenyl)-2-hydroxybutyl)imidazole (128.3 g) in a mixture of dimethyl sulfoxide (50 mL) and methylene chloride (200 mL) was added over a period of 20 minutes keeping the reaction mixture at temperatures below -65° C. After a further 15 minutes dry triethylamine (300 mL) was added rapidly and after 15 minutes the reaction mixture was allowed to warm to 0° C. Water (20 mL) was then added to the reaction mixture, the methylene chloride then removed by evaporation and the resulting slurry was then treated with water and filtered. The filter cake was washed well with ice-water, cold ethyl acetate and then dried in air to yield 118.0 g of 4-(4-chlorophenyl)-1-(imidazol-1-yl)butan-2-one. The hydrochloride salt crystallized from methanol/acetone had a melting point of 172.5°-174.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158949
Source datasetuspto-grants-1992_10
ORD IDord-f8e8e4a5050946c5a4b14e0ff1eaabc7
Source noteuspto-grants-1992_10