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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371912Generated: October 27, 2026

Potassium Carbonate → 1-(4-Chlorobenzoyl)-1-(3-chloro-1,2,4-triazol-1-yl)-cyclopropane

https://huagongshe.com/reaction/2371912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4-chloro-1-(4-chlorophenyl)butan-1-oneHCID 107167—
ReactantHCID 178478410HCID 178478410—
SolventAcetoneHCID 180—
Product1-(4-Chlorobenzoyl)-1-(3-chloro-1,2,4-triazol-1-yl)-cyclopropaneHCID 1469722790%

Reaction Steps

A mixture of 34 g (246 mmol) of potassium carbonate and 35 g (338 mmol) of 3-chloro-1,2,4-triazole in 130 ml of acetone is refluxed. To this mixture there is added dropwise a solution of 50 g (169 mmol) of 2-bromo-4-chloro-1-(4-chlorophenyl)-butan-1-one in 60 ml of acetone. The mixture is boiled under reflux for a further 8 hours, the solid residue is then filtered off with suction, and the solvent is stripped off under reduced pressure. The residue which remains is taken up in ethyl acetate. The solution is washed with water, dried over sodium sulphate and concentrated under reduced pressure. The residue which remains is chromatographed on silica gel using dichloromethane as the eluent. Concentration of the eluate by evaporation gives 42.9 g (90% of theory) of 1-(4-chlorobenzoyl)-1-(3-chloro-1,2,4-triazol-1-yl)-cyclopropane in the form of a solid of melting point 85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05096913
Source datasetuspto-grants-1992_03
ORD IDord-f0e212b1dd4042c7b53846df5a505cd3
Source noteuspto-grants-1992_03