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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24700생성일: 2026년 10월 23일

3,5-Dimethoxybenzaldehyde → 3,5-Dimethoxy-1-(1-propenyl)benzene

https://huagongshe.com/ko/reaction/24700

반응식

참여 물질

역할이름HCID투입량
반응물3,5-DimethoxybenzaldehydeHCID 81747—
반응물ButyllithiumHCID 178418339—
촉매Phosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
용매TetrahydrofuranHCID 8028—
생성물3,5-Dimethoxy-1-(1-propenyl)benzeneHCID 53900561—

반응 단계

Ethyltriphenylphosphonium bromide (4.69 g) was dissolved in anhydrous THF (70 mL) and the mixture cooled to 0-5° C. n-BuLi (5.05 mL of 2.5 M in hexane) was added dropwise and the resulting mixture was stirred at room temperature for 3 h. The mixture was cooled to −78° C. and a solution of 3,5-dimethoxybenzaldehyde (2 g) in anhydrous THF (14 mL) was added. The mixture was allowed to warm up to room temperature then stirred overnight. The mixture was concentrated, and the residue was taken up with AcOEt, washed with water and brine, dried (MgSO4), filtered and evaporated. The residue was purified by column chromatography (silica gel; eluent: hexane and AcOEt 10:1) to give 3,5-dimethoxy-1-(1-propenyl)benzene as a mixture of cis and trans isomers (2.15 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855843B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-e4d69c828dae4568959d5d61d5b064ec
출처 메모uspto-grants-2005_02