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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748780Generated: October 29, 2026

Dimethyl Sulfoxide → 5-((tert-Butyldimethylsilyl)oxy)pentanal

https://huagongshe.com/reaction/748780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-((Tert-butyldimethylsilyl)oxy)pentan-1-olHCID 3614318—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product5-((tert-Butyldimethylsilyl)oxy)pentanalHCID 1098770381.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere and at 0° C., dimethylsulfoxide (7.81 ml, 110 mmol), triethylamine (9.60 ml, 69.0 mmol), and a sulfur trioxide-pyridine complex (4.39 g, 27.6 mmol) were added to a dichloromethane solution (80 ml) of 5-(t-butyldimethylsilyloxy)pentanol (3.00 g, 13.8 mmol). The resulting mixture was stirred at 0° C. for 30 minutes and then, at room temperature for further 3 hours. After cooling to 0° C., a saturated aquoeus ammonium chloride solution was added. Dichloromethane was distilled off under reduced pressure. To the residue was added ethyl acetate. After the water layer was separated, the organic layer was washed with water and brine, dried over magnesium sulfate and then, concentrated. The residue thus obtained was subjected to chromatography on a silica gel column, and the fraction obtained from the hexane:ethyl acetate=20:1 eluate was concentrated, whereby the title compound (2.42 g, 11.2 mmol, 81%) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399775B2
Source datasetuspto-grants-2008_07
ORD IDord-c59df5db453846e3b9ec2d2902daf54c
Source noteuspto-grants-2008_07