Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609786Generated: October 29, 2026

Water → (S)-3-(t-butyldiphenylsilyloxy)-2-methylpropanal

https://huagongshe.com/reaction/1609786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl morpholine oxideHCID 82029—
Reactant1-Propanol, 3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-methyl-, (R)-HCID 11771817—
CatalystHCID 178419074HCID 178419074—
SolventDichloromethaneHCID 6344—
Product(S)-3-(t-butyldiphenylsilyloxy)-2-methylpropanalHCID 1178237297.5%

Reaction Steps

Under argon atmosphere, (R)-3-(t-butyldiphenylsilyloxy)-2-methylpropanol (48) (725 mg, 2.2 mmol) was dissolved in 40 ml of dry dichloromethane. MS-4A (30 mg), NMO (862 mg, 11.1 mmol) and TPAP (catalytic amount) were added to the resultant solution at 0° C., and the mixture was stirred for 15 min. The reaction mixture was further stirred overnight after the temperature was returned to room temperature. Subsequently, H2O was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with brine, dried over magnesium sulfate and evaporated. The obtained crude product was purified by column chromatography (21 g, 4% AcOEt-hexane) to obtain a colorless oily product (49) (700 mg, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982257B1
Source datasetuspto-grants-2006_01
ORD IDord-90f0904651e848bf81aa9c849b408204
Source noteuspto-grants-2006_01