HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260505Generated: November 1, 2026
Potassium Persulfate → HCID 54087854, compound
https://huagongshe.com/reaction/260505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 54296507 | HCID 54296507 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54087854 | HCID 54087854 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05527905 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-a77e8eff88624868b57ebfcf085f4d1d |
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| Source note | uspto-grants-1996_06 |
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