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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167720Generated: November 1, 2026

Piperazine → 1-Phenyl-4-piperazin-1-yl-cyclohexanecarbonitrile

https://huagongshe.com/reaction/1167720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-Oxo-1-phenylcyclohexanenitrileHCID 91282—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventEthylacetate methanolHCID 21584119—
Product1-Phenyl-4-piperazin-1-yl-cyclohexanecarbonitrileHCID 2299345640.2%

Reaction Steps

A mixture of 4-cyano-4-phenyl-cyclohexanone (0.23 g, 1.2 mmol) and piperazine (0.30 g, 3.5 mmol) in 20 ml of toluene was stirred at reflux for 2 h in presence of catalytic amount of p-toluenesulfonic acid. The reaction mixture was concentrated in vacuo to provide a white solid, which was redissolved in 20 ml of EtOH and stirred with NaBH4 (0.30 g, 80 mmol) for 12 h at 25° C. Reaction mixture was diluted with 100 ml of EtOAc and washed with brine several times. Organic layer was dried over MgSO4 and concentrated in vacuo, to provide oily residue, which was subjected to column chromatography (10% MeOH/EtOAc) to yield 0.13 g (40%) of the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620815B1
Source datasetuspto-grants-2003_09
ORD IDord-211fa3c26dfc4e46a0efeaf82d43ebfe
Source noteuspto-grants-2003_09