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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888623Generated: October 26, 2026

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

https://huagongshe.com/reaction/1888623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(Dimethyl-tert-butylsilyl)oxybutan-1-olHCID 186403—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-((Tert-butyldimethylsilyl)oxy)butanalHCID 10888976—

Reaction Conditions

Temperature-78 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501794B2
Source datasetuspto-grants-2013_08
ORD IDord-c4321c79b5934b9fa96458faa3b50545
Source noteuspto-grants-2013_08