HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781253Generated: October 30, 2026
Potassium Persulfate → HCID 19045180, compound
https://huagongshe.com/reaction/1781253
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 13505928 | HCID 13505928 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19045180 | HCID 19045180 | — |
Reaction Steps
1(b) 17.4 g of diethyl 1-(2,4-dimethoxybenzyl)-2-oxoazetidine-4,4-dicarboxylate (prepared as described above) were dissolved in a mixture of 350 ml of acetonitrile and 350 ml of water. 11.2 g of potassium persulfate and 37.4 g of dibasic potassium phosphate were then added to the resulting solution, and the mixture was stirred at 65° C. for 1 hour. At the end of this time, insoluble materials were filtered off and the filtrate was freed from the solvent by evaporation under reduced pressure. The residue was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, with an aqueous solution of sodium bicarbonate and with a saturated aqueous solution of sodium chloride, in that order. The solvent was then removed by distillation under reduced pressure, and the residue was purified by column chromatography through silica gel, eluted with a 1:2 by volume mixture of ethyl acetate and benzene, to give 5.72 g of diethyl 2-oxoazetidine-4,4-dicarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05633243 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-11519b9cfafb4d618293384b8bd77b54 |
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| Source note | uspto-grants-1997_05 |
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