Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1792973Erstellt: 25. Oktober 2026

Imidazole → 1-(4-((tert-Butyldimethylsilyl)oxy)-3,5-dimethoxyphenyl)ethanone

https://huagongshe.com/reaction/1792973

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktAcetosyringoneHCID 17198—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(4-((tert-Butyldimethylsilyl)oxy)-3,5-dimethoxyphenyl)ethanoneHCID 2202559381%

Reaktionsschritte

Ex-59A: To a solution of 4′-hydroxy-3′,5′-dimethoxyacetophenone (1 g, 5.1 mmol) in N,N-dimethylformamide were added tert-butyldimethylsilyl chloride (1,15 g, 7.6 mmol) and imidazole (0.69 g, 10.2 mmol). The mixture was stirred at room temperature overnight. Upon quenching with 1 M sulfuric acid solution, the mixture was extracted with dichloromethane. The organic phase was washed with saturated sodium bicarbonate and brine. It was dried and evaporated. Water (2 mL) was added to the residue, and the precipitate was filtered out and dried over an oil pump to give 1.28 g (81%) of 3′,5′-dimethoxy-4′-(tert-butyldimethylsiloxy)acetophenone as a white solid, m.p. 90-92° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07078431B2
Quelldatensatzuspto-grants-2006_07
ORD IDord-2095895f6d47499b941b0e13f624eeae
Quellennotizuspto-grants-2006_07