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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977620Generated: October 30, 2026

1-Phenylpiperazine → HCID 15288971, compound

https://huagongshe.com/reaction/1977620

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 wasted 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 numberUS06235732B1
Source datasetuspto-grants-2001_05
ORD IDord-5d11bccc7aff4b55b6fd7b9efa3c860e
Source noteuspto-grants-2001_05