Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704524Generated: October 27, 2026

Potassium Carbonate → 1-(4-Chlorobenzoyl)-1-(4-methylpiperazin-1-yl)-cyclopropane

https://huagongshe.com/reaction/704524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
Reactant1-MethylpiperazineHCID 53167—
Reactant2-Bromo-4-chloro-1-(4-chlorophenyl)butan-1-oneHCID 107167—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product1-(4-Chlorobenzoyl)-1-(4-methylpiperazin-1-yl)-cyclopropaneHCID 1371168450.3%

Reaction Steps

A solution of 29.6 g (0.1 mol) of 4-chlorophenyl 1-bromo-3-chloropropyl ketone in 30 ml of dimethylformamide is added dropwise to a mixture of 10.4 g of N-methyl piperazine and 14 g of potassium carbonate in 30 ml of dimethylformamide at room temperature. Stirring is continued for 3 hours, after which a solution of 9 g of potassium hydroxide in 30 ml of methanol is added dropwise. The reaction mixture is stirred for a further hour at 50 C. and evaporated down in vacuo. The residue is taken up in ethyl acetate/water, and the organic phase is separated off, washed with water, dried over sodium sulphate and evaporated down in vacuo. The residue is chromatographed over silica gel using chloroform/ethanol (97:3). 14 g (50.3% of theory) of 1-(4-chlorobenzoyl)-1-(4-methylpiperazin-1-yl)-cyclopropane are obtained as a reddish oil, which can be directly used further.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988382
Source datasetuspto-grants-1991_01
ORD IDord-c130781f8c794b21a72adedb7ba6921f
Source noteuspto-grants-1991_01