HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906613Generated: October 29, 2026
Trifluoroacetic acid → HCID 70373604, compound
https://huagongshe.com/reaction/1906613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 70373631 | HCID 70373631 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Anisole | HCID 7519 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 70373604 | HCID 70373604 | 101.9% |
Reaction Steps
1.55 g (4.34 mmol) of (3R,4R)-3-(1-t-butoxyformamido)-4-[(E)-2-carbamoylvinyl]-2-oxo-1-azetidinesulphonic acid sodium salt are dissolved in 5 ml of anisole, the solution is cooled to 0° C. and then treated with 5 ml of trifluoroacetic acid. The suspension obtained is stirred at 0° C. for 1 hour and subsequently at room temperature for 2 hours. The mixture is diluted with 100 ml of ether and 20 ml of n-hexane. The crystals obtained are filtered off and dried. The thus-obtained crude material is dissolved in 10 ml of water and chromatographed on MCI gel using water for the elution. 1.04 g (100%) of (3S,4S)-3-amino-4-[(E)-2-carbamoylvinyl]-2-oxo-1-azetidinesulphonic acid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04652651 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-e268af2e78b840788226a21bc0c0f68c |
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| Source note | uspto-grants-1987_03 |
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