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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354565Generated: October 31, 2026

Piperazine → 2-Fluoro-4-(piperazin-1-YL)benzonitrile

https://huagongshe.com/reaction/2354565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-DifluorobenzonitrileHCID 77545—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-Fluoro-4-(piperazin-1-YL)benzonitrileHCID 18760045—

Reaction Steps

Piperazine (20.0 g, 232.3 mmol) and K2CO3 (16.0 g, 118.5 mmol) are dissolved in CH3CN (85 ml). 2,4-Difluoro-benzonitrile (8.5 g, 61.1 mmol) is added and the mixture is stirred for 2 h at rt, then diluted with AcOEt and washed with water. The organic layer is separated, dried over Na2SO4 and evaporated. Excess piperazine is removed by MPLC (100 g silica gel, eluent CH2Cl2:MeOH 85:15). A second chromatographic purification (300 g silica gel, eluent toluene:EtOH:AcOH 4:4:1) yields the acetate salt of 2-fluoro-4-(piperazin-1-yl)-benzonitrile that is crystallized from AcOEt, filtered off and washed with ether. The free base is isolated by extraction with sat. aq. Na2CO3 solution/AcOEt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754719B2
Source datasetuspto-grants-2010_07
ORD IDord-572eca8e33804dc6baa1dcb7fc7ae72d
Source noteuspto-grants-2010_07