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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24700Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-DimethoxybenzaldehydeHCID 81747—
EduktButyllithiumHCID 178418339—
KatalysatorPhosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3,5-Dimethoxy-1-(1-propenyl)benzeneHCID 53900561—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855843B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-e4d69c828dae4568959d5d61d5b064ec
Quellennotizuspto-grants-2005_02