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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859627Generated: October 27, 2026

Water → 4-(4-Butyl-piperazin-1-yl)-butyronitrile

https://huagongshe.com/reaction/1859627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromobutyronitrileHCID 21412—
Reactant1-ButylpiperazineHCID 424322—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-(4-Butyl-piperazin-1-yl)-butyronitrileHCID 18626365—

Reaction Steps

In a 25 mL flask was placed 1-butyl-piperazine (712 mg, 5.0 mmol), 4-bromobutyronitrile (779 mg, 5.3 mmol) and potassium carbonate (687 mg, 5.0 mmol) suspended in acetonitrile (5 mL). The reaction mixture was stirred at rt for 12 h., followed by addition of H2O (20 mL) and extraction with ethyl acetate (3×25 mL). The combined organic phases were washed with brine (25 mL), dried (MgSO4) and evaporated to dryness to produce 0.89 g of crude 16 which was used without further purification in the synthesis of compound 17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528529B1
Source datasetuspto-grants-2003_03
ORD IDord-46096dcb360d44a88251e5b5f915d266
Source noteuspto-grants-2003_03