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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 396589Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/396589

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
PatentnummerUS06608101B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-9c03af725dbb419fb4274aa53f163c55
Quellennotizuspto-grants-2003_08