Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465183Generated: October 30, 2026

Acetic Acid → HCID 23705535, compound

https://huagongshe.com/reaction/465183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 23705552HCID 23705552—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventHCID 178418361HCID 178418361—
ProductHCID 23705535HCID 23705535—

Reaction Steps

In 70 ml of 30% methanol is dissolved 0.30 g of the sodium 3-[2-(2-carbobenzoxyaminomethylphenyl)acetamido]-2-oxoazetidine-1-sulfonate obtained in Example 80 followed by addition of 0.68 ml of 6% acetic acid and 75 mg of palladium black. The mixture is stirred in hydrogen gas streams at room temperature for 90 minutes, after which the catalyst is filtered off. The filtrate is concentrated under reduced pressure, followed by ddition of 30 ml of tetrahydrofuran. Then, under ice-cooling, 0.15 g of 1-chlorocarbonylimidazolid-2-one is added to the above tetrahydrofuran solution. The mixture is stirred for 90 minutes (its pH being maintained at 8.5 with a 1% aqueous solution of sodium hydrogen carbonate). The reaction mixture is adjusted to pH 6.5 with phosphoric acid, and the tetrahydrofuran is distilled off under reduced pressure. The residue is purified on an Amberlite XAD-II column to provide 0.24 g of sodium 3-[2-[2-(2-oxoimidazolidin-1 -yl)carbonylaminomethylphenyl]acetamido]-2-oxoazetidine-1-sulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04550105
Source datasetuspto-grants-1985_10
ORD IDord-e8a44902d7784a31afcd78c7538f394b
Source noteuspto-grants-1985_10