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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53665Erstellt: 25. Oktober 2026

1-Benzyl-4-piperidone → 1-Benzyl-4-propylidenepiperidine

https://huagongshe.com/reaction/53665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzyl-4-piperidoneHCID 19220—
EduktAllyltriphenylphosphonium bromideHCID 197740—
Edukt4-Benzylidenepiperidine hydrochlorideHCID 18539010—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzyl-4-propylidenepiperidineHCID 14966655—

Reaktionsschritte

Synthesis of 4-propenylidenepiperidine hydrochloride (1) In a stream of argon, 2.9 g (7.5 mmol) of allyltriphenylphosphonium bromide was suspended in 10 ml of anhydrous tetrahydrofurane, and thereto 4.3 ml of butyllithium was added dropwise under cooling with ice. After stirring the mixture at room temperature for 30 minutes, thereto was added dropwise a solution of 1 g (5.3 mmol) of 1-benzyl-4-piperidone in anhydrous tetrahydrofurane under cooling with ice and the obtained mixture was stirred at room temperature for 15 hours. The reaction solution was filtrated, and ethyl acetate 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 40 g of silica gel and eluted with ethyl acetate-hexane (1:1 to 1:3 ) to obtain 200 mg of 1-benzyl-4-propylidenepiperidine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05620994
Quelldatensatzuspto-grants-1997_04
ORD IDord-7d1104befd8b4dc2bad408f2229a11d9
Quellennotizuspto-grants-1997_04