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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003320Generated: October 31, 2026

Piperazine → 1-[4-(Propan-2-yl)piperazin-1-yl]ethan-1-one

https://huagongshe.com/reaction/1003320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantSodium IodideHCID 5238—
ReactantChloroformHCID 6212—
Reactant2-BromopropaneHCID 6358—
ReactantPotassium CarbonateHCID 11430—
SolventMethanolHCID 887—
Product1-[4-(Propan-2-yl)piperazin-1-yl]ethan-1-oneHCID 18796419—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 12.95 g of piperazine, 0.75 g of sodium iodide and 3.46 g of potassium carbonate were added successively 25 ml of methanol and 6.15 g of 2-bromopropane and the mixture was stirred at 60° C. for 4 hours. After the addition of chloroform and washing with a saturated aqueous solution of sodium chloride, the mixture was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, 12 ml of acetic anhydride was slowly added and the mixture was stirred at room temperature for 2.5 hours. The reaction solution was poured into ice and chloroform was added and the mixture was neutralized with sodium carbonate. After extracting with chloroform, the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue thus obtained was chromatographed over a silica gel column. The solvent was distilled off and the residue was allowed to stand overnight. The diacetylpiperazine thus precipitated out was filtered off to afford 7.26 g of the title compound as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046201
Source datasetuspto-grants-2000_04
ORD IDord-ab004de9e77242eeaf0b66d58115bfd2
Source noteuspto-grants-2000_04