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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683117Generated: November 1, 2026

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

https://huagongshe.com/reaction/1683117

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 (25.2g, 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 numberUS05635510
Source datasetuspto-grants-1997_06
ORD IDord-7383def6498e4f419160f8e0b2a8f8b7
Source noteuspto-grants-1997_06