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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343717Generated: October 31, 2026

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

https://huagongshe.com/reaction/343717

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 numberUS05861416
Source datasetuspto-grants-1999_01
ORD IDord-7196131bc85b48c180eb5cb7a5f2c8d7
Source noteuspto-grants-1999_01