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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53665생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/53665

반응식

참여 물질

역할이름HCID투입량
반응물1-Benzyl-4-piperidoneHCID 19220—
반응물Allyltriphenylphosphonium bromideHCID 197740—
반응물4-Benzylidenepiperidine hydrochlorideHCID 18539010—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-4-propylidenepiperidineHCID 14966655—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620994
출처 데이터셋uspto-grants-1997_04
ORD IDord-7d1104befd8b4dc2bad408f2229a11d9
출처 메모uspto-grants-1997_04