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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745387Generated: October 30, 2026

Trifluoroacetic acid → HCID 131712318, compound

https://huagongshe.com/reaction/745387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131712317HCID 131712317—
SolventAnisoleHCID 7519—
ProductHCID 131712318HCID 13171231889.8%

Reaction Steps

Trifluoroacetic acid (40 ml.) was added to a suspension of 4-nitrobenzyl 7-[2-(2-formamidothiazol-4-yl)-2-t-butoxycarbonylmethoxyiminoacetamido]-3-cephem-4-carboxylate (syn isomer, 10 g.) in anisole (10 ml.) at 5° C., and stirred at room temperature for 70 minutes. After evaporating the solvent from the resultant mixture in vacuo, the residue was triturated with diethyl ether. The precipitates were collected by filtration and dried to give 4-nitrobenzyl 7-[2-(2-formamidothiazol-4-yl)-2-carboxymethoxyiminoacetamido]-3-cephem-4-carboxylate (syn isomer, 8.2 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04598147
Source datasetuspto-grants-1986_07
ORD IDord-e246fc6a07f144a88c82fbeca04f3d2c
Source noteuspto-grants-1986_07