HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Persulfate → HCID 54342386, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 131715082 | HCID 131715082 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54342386 | HCID 54342386 | 37.3% |
Reaction Steps
4.0 g (8.9 mmol) of ethyl rac-cis-3-(1-t-butoxyformamido)-1-(2,4-dimethoxybenzyl)-β-methyl-2-oxo-4-azetidineacrylate are dissolved in 300 ml of acetonitrile and the solution is treated at 90°-95° C. with 3.86 g (14.3 mmol) of potassium peroxydisulphate and 2.31 (13.3 mmol) of potassium hydrogen sulphate for 2 hours. The organic solvent is removed by evaporation and the aqueous phase is extracted with chloroform. The combined organic phases are washed with aqueous sodium chloride solution and dried over sodium sulphate. The solution is evaporated and the residue is chromatographed on silica gel using ethyl acetate for the elution. 990 mg (37%) of t-butyl 4-[2-(ethoxycarbonyl)-1-methylvinyl]-2-oxo-3-azetidinecarbamate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04948898 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-8bbb2952879b4e37a8b756b010e65f4e |
| Source note | uspto-grants-1990_08 |