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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258778Generated: November 2, 2026

Benzyl Bromide → 1-Benzyl-4-cyano-4-phenylpiperidine

https://huagongshe.com/reaction/2258778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Phenylpiperidine-4-carbonitrile hydrochlorideHCID 3084973—
SolventOxolane--water (1/1)HCID 21881883—
Product1-Benzyl-4-cyano-4-phenylpiperidineHCID 191408—

Reaction Steps

4-Phenyl-4-cyano-piperidine hydrochloride (10 g, 44.9 mmol), Benzyl bromide (5.4 mL, 45.4 mmol), and potassium carbonate (25.2 g, 182.3 mmol) were combined in THF/water (80 mL/20 mL). After 18 hours the reaction mixture was partitioned between water and dichloromethane. The organic layer was separated and extracted with water, dried over MgSO4, filtered and evaporated in vacuo to give a residue. The residue was recrystallized from hexane to give 4-phenyl-4-cyano-1-benzyl-piperidine as a solid: mp=73°-74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05661160
Source datasetuspto-grants-1997_08
ORD IDord-21dabd8897fd4fceaf054db98662158e
Source noteuspto-grants-1997_08