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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723880Generated: November 1, 2026

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

https://huagongshe.com/reaction/1723880

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 numberUS07485651B2
Source datasetuspto-grants-2009_02
ORD IDord-2ab57e16d1b343629576b0b2a7dcac71
Source noteuspto-grants-2009_02