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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162341Generated: October 27, 2026

Chloroacetonitrile → 2-(4-Benzylpiperazin-1-yl)acetonitrile

https://huagongshe.com/reaction/1162341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantSodium CarbonateHCID 10340—
Reactant1-BenzylpiperazineHCID 75994—
SolventAcetoneHCID 180—
Product2-(4-Benzylpiperazin-1-yl)acetonitrileHCID 385572180%

Reaction Steps

To a suspension of 1-benzylpiperazine (18 g) and sodium carbonate (8.3 g) in acetone (50 ml) was added chloroacetonitrile (12 g) under ice-cooling, and mixed at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, to the residue were added water and diethyl ether, and the organic layer was collected by separation. The organic layer was washed with water and dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified with silica gel column (ethyl acetate) to obtain the title compound as pale yellow liquid (17 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820673B2
Source datasetuspto-grants-2010_10
ORD IDord-49746a654edc41f09f637016a9bc8aa1
Source noteuspto-grants-2010_10