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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260505Generated: November 1, 2026

Potassium Persulfate → HCID 54087854, compound

https://huagongshe.com/reaction/260505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PersulfateHCID 24412—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 54296507HCID 54296507—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 54087854HCID 54087854—

Reaction Conditions

Temperature70 °C

Reaction Steps

3(a) 14 g of benzyl 1-(2,4-dimethoxybenzyl)-3-[(R)-1-hydroxyethyl]-2-oxoazetidine-4-carboxylate [which had been synthesized according to a procedure similar to that described in Tetrahedron 46, 1795 (1984)] were dissolved in a mixture of 420 ml of acetonitrile and 420 ml of water. 66.1 g of potassium persulfate and 23.3 g of dibasic potassium phosphate were added to the solution, and the mixture was stirred at 70° C. for 60 minutes. At the end of this time, insoluble materials were filtered off, and the filtrate was concentrated by evaporation under reduced pressure. The residue was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and freed from the solvent by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel to afford 6.1 g of benzyl 3-[(R)-1-hydroxyethyl]-2-oxoazetidine-4-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527905
Source datasetuspto-grants-1996_06
ORD IDord-a77e8eff88624868b57ebfcf085f4d1d
Source noteuspto-grants-1996_06