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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592747Generated: October 31, 2026

Piperazine → 2-(Piperazin-1-yl)-4-trifluoromethylbenzonitrile

https://huagongshe.com/reaction/1592747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-Fluoro-4-(trifluoromethyl)benzonitrileHCID 518973—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product2-(Piperazin-1-yl)-4-trifluoromethylbenzonitrileHCID 1795232496.6%

Reaction Steps

To a solution of piperazine (13.7 g, 159 mmol) in 20 mL DMSO was added 2-fluoro-4-trifluoromethylbenzonitrile (10 g, 52.9 mmol). After stirring overnight, the solution was diluted with 200 mL of EtOAc, washed with water and brine, and then dried (Na2SO4), filtered and concentrated to afford about 13.0 g (51.1 mmol, 96%) of 4-(2-cyano-5-trifluoromethyl-phenyl)piperazine. LRMS (ESI+): 256.1 [M+1]. The tide compound was prepared from 4-(2-cyano-5-trifluoromethyl-phenyl)piperazine in the same manner as described in Preparation 67A except that dimethyl amine was used to displace the mesylate. LRMS (ESI+): 388.1 [M+1]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291619B2
Source datasetuspto-grants-2007_11
ORD IDord-85ec3716fef7426f992015cf15a51efb
Source noteuspto-grants-2007_11