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HRID 24700作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DimethoxybenzaldehydeHCID 81747—
反応物ButyllithiumHCID 178418339—
触媒Phosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
溶媒TetrahydrofuranHCID 8028—
生成物3,5-Dimethoxy-1-(1-propenyl)benzeneHCID 53900561—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855843B2
出典データセットuspto-grants-2005_02
ORD IDord-e4d69c828dae4568959d5d61d5b064ec
出典メモuspto-grants-2005_02