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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074363Generated: November 2, 2026

Trifluoroacetic acid → HCID 131716074, compound

https://huagongshe.com/reaction/1074363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 131716076HCID 131716076—
SolventDichloromethaneHCID 6344—
SolventAnisoleHCID 7519—
ProductTrifluoroacetic acidHCID 6422—
ProductHCID 131716074HCID 13171607490%

Reaction Steps

To a suspension of benzhydryl 7β-[2-cyclopropyloxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-(4-carbamoyl-1-pyridinio)methyl-3-cephem-4-carboxylate trifluoroacetate (syn isomer) (2.7 g) in a mixture of anisol (5 ml) and methylene chloride (10 ml) was added trifluoroacetic acid (10 ml) under ice-cooling. The mixture was stirred at the same temperature for 30 minutes. The mixture was poured into diisopropyl ether (800 ml) and the resulted precipitate was collected and dried over phosphorus pentoxide to give trifluoroacetic acid salt of 7β-[2-cyclopropyloxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-(4-carbamoyl-1-pyridinio)methyl-3-cephem-4-carboxylate (syn isomer) (1.63 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04973699
Source datasetuspto-grants-1990_11
ORD IDord-39259ef25f9345e28312bf8f0ceb1a60
Source noteuspto-grants-1990_11