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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434873Generated: October 29, 2026

Trifluoroacetic acid → HCID 131712706, compound

https://huagongshe.com/reaction/434873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantTrifluoroacetateHCID 84468—
ReactantHCID 131712707HCID 131712707—
SolventDichloromethaneHCID 6344—
ProductHCID 131712706HCID 131712706—

Reaction Steps

To a solution of benzhydryl 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-(4-methyl-1-piperazinyl)carbonyloxymethyl-3-cephem-4-carboxylate.trifluoroacetate (syn isomer) (1.4 g ) in methylene chloride (30 ml) were added anisole (1.4 ml) and trifluoroacetic acid (1.83 ml) with stirring under ice-cooling and the stirring was continued for 4 hours at 5° C. The reaction mixture was evaporated and the residual oil was pulverized in diethyl ether, collected by filtration and then dried to give 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-(4-methyl-1-piperazinyl)carbonyloxymethyl-3-cephem-4-carboxylic acid.trifluoroacetate (syn isomer) (1.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399278
Source datasetuspto-grants-1983_08
ORD IDord-99cfab19d69f4780bae731a769a0505f
Source noteuspto-grants-1983_08