Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847706Generated: October 30, 2026

HCID 12784140, compound → 7beta-Phenoxyacetamido-3-methoxy-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/847706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12784140HCID 12784140—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMeOH tetrahydrofuranHCID 21899815—
Product7beta-Phenoxyacetamido-3-methoxy-3-cephem-4-carboxylic acidHCID 12784142—

Reaction Steps

A solution of 250 mg (0.5 mmol) of 7β-phenoxyacetamido-3-methoxy-3-cephem-4-carboxylic acid p-nitrobenzyl ester in 2 ml of methanol/tetrahydrofurane, 1:1, is added to a mixture of 5% palladium/charcoal in 2 ml of the same solvent, which mixture has been prehydrogenated for one hour under atmospheric pressure, and the reaction mixture is hydrogenated for 3 hours at room temperature and under atmospheric pressure. After this time, about 90% of the calculated amount of hydrogen has been taken up. The catalyst is filtered off and the filtrate is evaporated in vacuo. The residue is taken up in 10 ml of methylene chloride and extracted with twice 10 ml of 5% strength aqueous sodium bicarbonate solution. The combined bicarbonate extracts are neutralised at 0° C. with dilute hydrochloric acid and extracted with 3 times 10 ml of methylene chloride. The organic phase is dried over sodium sulphate and freed from the solvent in vacuo. After crystallisation from chloroform/pentane, the residue gives 7β-phenoxyacetamido-3-methoxy-3-cephem-4-carboxylic acid of melting point 173°-174° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04293462
Source datasetuspto-grants-1981_10
ORD IDord-bec4f9101ab642d8b0dc5b5a95b4efa5
Source noteuspto-grants-1981_10