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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53664Generated: October 26, 2026

1-Benzyl-4-piperidone → 1-Benzyl-4-benzylidenepiperidine

https://huagongshe.com/reaction/53664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
Reactant4-Benzylidenepiperidine hydrochlorideHCID 18539010—
ReactantButyllithiumHCID 178418339—
CatalystBenzyltriphenylphosphonium chlorideHCID 70671—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-4-benzylidenepiperidineHCID 21843364—

Reaction Steps

Synthesis of 4-benzylidenepiperidine hydrochloride (1) In a stream of argon, 49.0 g (126 mmol) of benzyltriphenylphosphonium chloride was suspended in 100 ml of anhydrous tetrahydrofurane, and thereto 86 ml of butyllithium was added dropwise under cooling with ice. After stirring the mixture at room temperature for 1 hour, thereto was added dropwise a solution of 1-benzyl-4-piperidone in anhydrous tetrahydrofurane under cooling with ice and the obtained mixture was refluxed with heating for 15 hours. The reaction solution was filtrated, and diethyl ether and water were added to the filtrate, and the organic phase was taken out. The organic phase was washed with water and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the resulting oily matter was subjected to a column chromatography using 1 kg of silica gel and eluted with ethyl acetate-hexane (1:100 to 3:100) to obtain 22.6 g of 1-benzyl-4-benzylidenepiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620994
Source datasetuspto-grants-1997_04
ORD IDord-76a3d0f5602843f29b9987c0655944f4
Source noteuspto-grants-1997_04