HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 131715083, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131715084 | HCID 131715084 | — |
| Solvent | Anisole | HCID 7519 | — |
| Solvent | Diethylether hexane | HCID 21584099 | — |
| Product | HCID 131715083 | HCID 131715083 | 66.3% |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
1.755 g (4.38 mmol) of rac-cis-3-(1-t-butoxyformamido)-4-[(Z)-2-(ethoxycarbonyl)-1-methylvinyl]-2-oxo-1-azetidinesulphonic acid sodium salt are dissolved in 7.5 ml of anisole and the solution is treated at -20° C. with 10 ml of trifluoroacetic acid. After stirring at -20° C. for 30 minutes and then at room temperature for a further 3 hours, the solution is diluted with 300 ml of ether/n-hexane (1:1). The crystals obtained are filtered off, dissolved in 10 ml of water and chromatographed on MCI gel. 808 mg (60%) of rac-cis-3-amino-4-[(Z)-2-(ethoxycarbonyl)-1-methylvinyl]-2-oxo-1-azetidinesulphonic acid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04948898 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-f86411cb718b4bf0a16aa313d873b21a |
| Source note | uspto-grants-1990_08 |