돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1737431생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1737431

반응식

참여 물질

역할이름HCID투입량
반응물1-Benzyl-4-piperidoneHCID 19220—
반응물Allyltriphenylphosphonium bromideHCID 197740—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-4-propylidenepiperidineHCID 1496665517.5%

반응 단계

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 a 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 번호US05962476
출처 데이터셋uspto-grants-1999_10
ORD IDord-7845f52371564048adaa27537172da7e
출처 메모uspto-grants-1999_10