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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737093Generated: October 25, 2026

Acetonitrile → 1-(4-Bromo-benzyl)-3-phenyl-piperidine

https://huagongshe.com/reaction/737093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant2-PhenylpiperidineHCID 103020—
Product1-(4-Bromo-benzyl)-3-phenyl-piperidineHCID 5784957154%

Reaction Steps

5.632 g of 4-Bromobenzyl bromide and 2.422 g of 2-Phenylpiperidine (Array) in 50 mL of acetonitrile were stirred at room temperature and 6.229 g of potassium carbonate was added. The reaction was stirred at room temperature overnight. The solution was filtered through Celite and concentrated in vacuo to afford a brown solid. Purification was done by flash chromatography to afford product. Wt:0.908 g, 54% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595397B2
Source datasetuspto-grants-2009_09
ORD IDord-34fa2b02ab2e469ea65d7e888a05af06
Source noteuspto-grants-2009_09