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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53664생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1-Benzyl-4-piperidoneHCID 19220—
반응물4-Benzylidenepiperidine hydrochlorideHCID 18539010—
반응물ButyllithiumHCID 178418339—
촉매Benzyltriphenylphosphonium chlorideHCID 70671—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-4-benzylidenepiperidineHCID 21843364—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620994
출처 데이터셋uspto-grants-1997_04
ORD IDord-76a3d0f5602843f29b9987c0655944f4
출처 메모uspto-grants-1997_04