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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 253613Erstellt: 24. Oktober 2026

Dimethyl Sulfoxide → 4-((Tert-butyldimethylsilyl)oxy)butanal

https://huagongshe.com/de/reaction/253613

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt4-(Dimethyl-tert-butylsilyl)oxybutan-1-olHCID 186403—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-((Tert-butyldimethylsilyl)oxy)butanalHCID 10888976—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To CH2Cl2 (150 mL) at −78° C. were added oxalyl chloride (6.83 g, 53.8 mmol) and dry DMSO (8.41 g, 108 mmol), dropwise. After 5 min, 4-(tert-butyldimethylsilyloxy)butan-1-ol (10 g, 48.9 mmol) in CH2Cl2 (5 mL) was added dropwise. The mixture was stirred for an additional 30 min at −78° C., and Et3N (24.8 g, 245 mmol) was added. The mixture was then allowed to warm to room temperature over 30 min. After stirring for 3 hrs, 100 mL of water was added. The phases were separated, and the aqueous phase was extracted three times with 100 mL of diethyl ether. The combined organic phases were washed successively with 50 mL of aqueous 1% HCl, 50 mL of water, 50 mL of aqueous 5% NaHCO3 and 50 mL of saturated aqueous NaCl. The organic layer was dried over MgSO4, and the solvent was removed under reduced pressure, to provide the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07872033B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-33671c5596534572bc1e0b44c412f9da
Quellennotizuspto-grants-2011_01