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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1016701Erstellt: 24. Oktober 2026

Triethylamine → (S)-Glycidoxy-t-butyldimethylsilane

https://huagongshe.com/de/reaction/1016701

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
Edukt(+)-GlycidolHCID 5460455—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-Glycidoxy-t-butyldimethylsilaneHCID 1095430781,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of (R)-glycidol (5 g, 67.5 mmol) in dry dichloromethane containing triethylamine (10.3 ml, 74 mmol) cooled down to 0° C., was added a solution of tert-butyldimethylsilyl chloride (11.2 g, 74 mmol) in dry dichloromethane (30 ml). Then DMAP ( 0.33 g, 2.7 mmol) was added. The mixture was allowed to warm up to room temperature and stirred for 5 hours. The triethylammonium chloride crystals were filtered out and washed with dichloromethane (2×10 ml). The organic solution was washed with brine (2×50 ml) and dried over anhydrous sodium sulfate. The solution was concentrated and passed though a short silica gel column to remove polar impurities, and eluted with hexane/ethyl acetate (3:2). After removing the solvent, a colourless oil was collected and dried in vacuo to provide pure (S)-glycidyl-tert-butyldimethylsilyl ether (10.3 g, 81.2%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06476216B1
Quelldatensatzuspto-grants-2002_11
ORD IDord-94214aef4c294816994514ae999b42f5
Quellennotizuspto-grants-2002_11