Reaktion #81942

Reaktionsgleichung

4-benzylidenepiperidine hydrochloride

butyllithium

1-benzyl-4-piperidone

→

1-benzyl-4-benzylidenepiperidine

Lösungsmittel

tetrahydrofurane

tetrahydrofurane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturunder cooling with ice
2. 2
   Temperaturunder cooling with ice
3. 3
   Temperaturthe obtained mixture was refluxed
4. 4
   Temperaturwith heating for 15 hours
5. 5
   FiltrationThe reaction solution was filtrated
6. 6
   workup.ADDITIONdiethyl ether and water were added to the filtrate
7. 7
   WaschenThe organic phase was washed with water
8. 8
   Trocknena saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate
9. 9
   SonstigeThe solvent was removed under reduced pressure
10. 10
    Wascheneluted with ethyl acetate-hexane (1:100 to 3:100)

Vorschrift

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.

Quelle