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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744870Generated: October 30, 2026

Sodium Iodide → HCID 70194500, compound

https://huagongshe.com/reaction/744870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium trifluoroacetateHCID 2724268—
ReactantHCID 70195797HCID 70195797—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 70194500HCID 70194500—

Reaction Steps

To a solution of tert-butyl 7-phenylacetamido-3-bromomethyl-3-cephem-4-carboxylate-1-oxide (76.1 g; 0.158 mol) in N,N-dimethylformamide (350 ml), ammonium trifluoroacetate (41.3 g; 0.316 mol) and sodium iodide (23.6 g; 0.158 mol) were added, followed by stirring at room temperature. The reaction mixture was added with ammonium trifluoroacetate (10.3 g; 0.079 mol) upon an elapsed time of 4 hours and 35 minutes from the initiation of the stirring and then with sodium iodide (11.8 g, 0.079 mol) upon an elapsed time of 8 hours and 5 minutes after the initiation of the stirring. Stirring was continued at room temperature for 24 hours and 25 minutes in total. The reaction mixture was poured into a mixture of ethyl acetate, and water and the ethyl acetate layer was collected. The water layer was extracted twice with ethyl acetate. Ethyl acetate layers were combined together, successively washed with water and saturated aqueous sodium chloride solution, and then dried over magnesium sulfate. The solvent was then distilled off under reduced pressure, whereby tert-butyl 7-phenylacetamido-3-hydroxymethyl-3-cephem-4-carboxylate-1-oxide was obtained (yield: 63.5 g; 6.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559225
Source datasetuspto-grants-1996_09
ORD IDord-0edf3332e279457abd4ecd6ea6b01e19
Source noteuspto-grants-1996_09