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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635833Generated: October 30, 2026

1-Phenylpiperazine → HCID 15288971, compound

https://huagongshe.com/reaction/635833

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
Reactant2-MethoxybenzaldehydeHCID 8658—
ReactantPotassium CyanideHCID 9032—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 15288971HCID 1528897176%

Reaction Conditions

Temperature0 °C

Reaction Steps

6.5 g (40 mmol) of 1-phenylpiperazine are dissolved in 40 ml of 1N-hydrochloric acid and mixed with a solution of 5.4 g (40 mmol) of 2-methoxybenzaldehyde in 60 ml of ether. The mixture is cooled to 0° C., a solution of 2.5 g (40 mmol) potassium cyanide in 30 ml of water is slowly added dropwise, with stirring, and the mixture is stirred overnight at ambient temperature. Then the organic phase is separated off (any product already precipitated is removed by suction filtration beforehand). The aqueous phase is washed three times with 50 ml of ether, the organic phases are combined and dried over sodium sulfate. The solvent is eliminated in vacuo and the residue is stirred with cyclohexane and suction filtered. 9.3 g of (2-Methoxyphenyl)-(4-phenylpiperazine-1-yl)-acetonitrile are obtained (76% yield) as an almost colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06191135B1
Source datasetuspto-grants-2001_02
ORD IDord-2f3ef22692c243b784596657aa2e384e
Source noteuspto-grants-2001_02