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HRID 861947作成日:2026年10月27日

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

https://huagongshe.com/reaction/861947

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Allyltriphenylphosphonium bromideHCID 197740—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzyl-4-propylidenepiperidineHCID 1496665517.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05716969
出典データセットuspto-grants-1998_02
ORD IDord-6f410f843aaa428a82d003f5d50caf8b
出典メモuspto-grants-1998_02