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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65439Generated: October 23, 2026

Potassium Phosphate, Dibasic → 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone

https://huagongshe.com/en/reaction/65439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, DibasicHCID 24450—
ReactantSodium PersulfateHCID 62655—
Reactant1-p-methoxybenzyl-3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinoneHCID 18604772—
CatalystFerrous sulfate heptahydrateHCID 62662—
CatalystCupric acetate monohydrateHCID 165397—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinoneHCID 18604774—

Reaction Steps

A solution of 68.3 mg (0.2 mmol) of 1-p-methoxybenzyl-3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone in 4 ml of acetonitrile is added to a solution of 428 mg (1.8 mmol) of sodium peroxydisulphate, 174 mg (1 mmol) of dipotassium hydrogen phosphate, 1 mg of iron(II) sulphate heptahydrate and 2 mg of copper(II) acetate hydrate in 4 ml of water. The mixture is stirred for 2 hours under an argon atmosphere at a bath temperature of 65°. The resulting mixture is then concentrated to half its volume under reduced pressure and extracted with ethyl acetate. The extract is triturated with methylene chloride and ether and the pure title compound is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614614
Source datasetuspto-grants-1986_09
ORD IDord-139ed6457cd64e2e9fcb010d4805aeea
Source noteuspto-grants-1986_09