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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465172Generated: October 30, 2026

Diazomethane → HCID 12784140, compound

https://huagongshe.com/reaction/465172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
Reactant7beta-Phenoxyacetamido-3-hydroxy-3-cephem-4-carboxylic acid p-nitrobenzyl esterHCID 54716794—
SolventChloroformHCID 6212—
ProductHCID 12784140HCID 12784140—

Reaction Conditions

Temperature0 °C

Reaction Steps

3 ml of an ethereal diazomethane solution (0.5 molar, 1.5 equivalents) are added in the course of about 10 minutes to a solution, cooled to 0° C., of 485 mg of 7β-phenoxyacetamido-3-hydroxy-3-cephem-4-carboxylic acid p-nitrobenzyl ester in 10 ml of dry chloroform. The pale yellow solution is stirred for 1 hour at 0° C., flushed with nitrogen in order to remove excess diazomethane and concentrated in vacuo. The residue is recrystallised from methylene chloride and gives 7β-phenoxyacetamido-3-methoxy-3-cephem-4-carboxylic acid p-nitrobenzyl ester of melting point 140.5°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04550162
Source datasetuspto-grants-1985_10
ORD IDord-5c0d638caf224144be72a037b27d71dd
Source noteuspto-grants-1985_10