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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23710Erstellt: 23. Oktober 2026

Imidazole → 4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehyde

https://huagongshe.com/de/reaction/23710

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktHexaneHCID 8058—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
EduktBenzaldehyde, 4-(2-hydroxyethoxy)-HCID 89178—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehydeHCID 5795610149,9%

Reaktionsschritte

To 4-(2-hydroxyethoxy)benzaldehyde (commercial, 0.5 g, 3 mmol) dissolved in DMF (10 mL) is added imidazole (0.4 g, 6 mmol) and tert-butyldimethylsilylchloride (0.53 g, 3.5 mmol). Reaction mixture is stirred for 20 h. at room temperature. TLC analysis (hexane:ethyl acetate,7:3) shows small amounts of unreacted starting material. Additional tert-butyldimethylsilylchloride (0.25 g, 1 mmol) is added and stirring continued for 16 h. The reaction is quenched with saturated aqueous ammonium chloride (20 mL) and diluted further with ethyl ether (20 mL). Aqueous layer is separated and extracted thrice with ether (10 mL). Combined organics dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue is purified by flash chromatography on silica gel using a gradient of 2% to 5% ethyl acetate in hexanes to provide 0.42 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852731B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-80c3f0ea60a240ea855be153730b5b6d
Quellennotizuspto-grants-2005_02