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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906613Generated: October 29, 2026

Trifluoroacetic acid → HCID 70373604, compound

https://huagongshe.com/reaction/1906613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70373631HCID 70373631—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventAnisoleHCID 7519—
SolventHexaneHCID 8058—
ProductHCID 70373604HCID 70373604101.9%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04652651
Source datasetuspto-grants-1987_03
ORD IDord-e268af2e78b840788226a21bc0c0f68c
Source noteuspto-grants-1987_03