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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53664Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/53664

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzyl-4-piperidoneHCID 19220—
Edukt4-Benzylidenepiperidine hydrochlorideHCID 18539010—
EduktButyllithiumHCID 178418339—
KatalysatorBenzyltriphenylphosphonium chlorideHCID 70671—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzyl-4-benzylidenepiperidineHCID 21843364—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05620994
Quelldatensatzuspto-grants-1997_04
ORD IDord-76a3d0f5602843f29b9987c0655944f4
Quellennotizuspto-grants-1997_04