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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255667Generated: October 29, 2026

Potassium Persulfate → (3S)-3-[(1R)-1-(t-butyldimethylsilyloxy)ethyl]azetidin-2-one

https://huagongshe.com/reaction/2255667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PersulfateHCID 24412—
ReactantPotassium Phosphate, DibasicHCID 24450—
Reactant(3S)-3-[(1R)-1-(t-butyldimethylsilyloxy)ethyl]-1-(4-methoxybenzyl)azetidin-2-oneHCID 54758409—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(3S)-3-[(1R)-1-(t-butyldimethylsilyloxy)ethyl]azetidin-2-oneHCID 1013079544.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of (3S)-3-[(1R)-1-(t-butyldimethylsilyloxy)ethyl]-1-(4-methoxybenzyl)azetidin-2-one (2.45 g), potassium persulfate (4.73 g) and dipotassium hydrogen phosphate (3.66 g) in acetonitrile (35 ml) and water (30 ml) was stirred at 70° C. for 2 hours. The mixture was evaporated and the residue was extracted with ethyl acetate. The extract was washed with 1N hydrochloric acid, saturated aqueous sodium hydrogencarbonate, water and an aqueous sodium chloride in turn, and then dried over magnesium sulfate. The resultant solution was evaporated and the residue was column-chromatographed on silica gel (eluent : a mixture of hexane and ethyl acetate, 3:1) to give (3S)-3-[(1R)-1-(t-butyldimethylsilyloxy)ethyl]azetidin-2-one (0.71 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05241064
Source datasetuspto-grants-1993_08
ORD IDord-4658228a3c334de3b89d9514b0e19657
Source noteuspto-grants-1993_08