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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26088생성일: 2026년 10월 26일

4-Pyridinecarboxaldehyde → 4-(3-Methoxyphenyl)-1-(4-pyridyl)-1-pentene

https://huagongshe.com/reaction/26088

반응식

참여 물질

역할이름HCID투입량
반응물4-PyridinecarboxaldehydeHCID 13389—
반응물Sodium hydrideHCID 24758—
반응물3-(3-Methoxyphenyl)butyltriphenylphosphonium bromideHCID 20496878—
용매Dimethyl SulfoxideHCID 679—
용매TetrahydrofuranHCID 8028—
생성물4-(3-Methoxyphenyl)-1-(4-pyridyl)-1-penteneHCID 54047177—

반응 단계

A mixture of 3-(3-methoxyphenyl)butyl triphenylphosphonium bromide (17.5 g., 35.4 mmoles) in dimethylsulfoxide (50 ml.) is added to 4-pyridinecarboxaldehyde (3.79 g., 35.4 mmoles) in tetrahydrofuran (40 ml.). The resulting mixture is then added dropwise to a slurry of 50% sodium hydride (1.87 g., 39 mmoles) in tetrahydrofuran (20 ml.) under a nitrogen atmosphere at 0°-5° C. Following completion of addition, the mixture is stirred for one hour at 0°-5° C. and then concentrated under reduced pressure. The concentrate is diluted with water (200 ml.) and then acidified with 6N HCl. The aqueous acid solution is extracted with benzene (4 × 50 ml.). It is then made basic and extracted with ethyl acetate (3 × 50 ml.). Evaporation of the combined extracts after drying (MgSO4) affords 4-(3-methoxyphenyl)-1-(4-pyridyl)-1-pentene as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04147872
출처 데이터셋uspto-grants-1979_04
ORD IDord-82dad07c0bb24612af1f92dd1c4e46fd
출처 메모uspto-grants-1979_04