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HRID 53664作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物1-Benzyl-4-piperidoneHCID 19220—
反応物4-Benzylidenepiperidine hydrochlorideHCID 18539010—
反応物ButyllithiumHCID 178418339—
触媒Benzyltriphenylphosphonium chlorideHCID 70671—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzyl-4-benzylidenepiperidineHCID 21843364—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05620994
出典データセットuspto-grants-1997_04
ORD IDord-76a3d0f5602843f29b9987c0655944f4
出典メモuspto-grants-1997_04