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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67847Generated: October 30, 2026

Hydrochloric Acid → p-Nitrobenzyl 3-oxo-7-phenoxyacetamidocepham-4-carboxylate

https://huagongshe.com/reaction/67847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactantp-Nitrobenzyl alpha-[4-mercapto-3-phenoxyacetamido-2-oxoazetidin-1-yl]-alpha-(2-bromo-1-hydroxyethylidene)acetateHCID 86735550—
SolventDichloromethaneHCID 6344—
Productp-Nitrobenzyl 3-oxo-7-phenoxyacetamidocepham-4-carboxylateHCID 7054778674%

Reaction Steps

A solution of p-nitrobenzyl α-[4-mercapto-3-phenoxyacetamido-2-oxoazetidin-1-yl]-α-(2-bromo-1-hydroxyethylidene)acetate prepared by the method of Example 4-III (2) (70 mg) in a mixture of methylene chloride (2 ml), methanol (2 ml), and 10% hydrochloric acid (0.3 ml) is stirred at room temperature for 2 hours. The reaction mixture is poured into ice water, and is extracted with methylene chloride. The extract solution is washed with water, dried over magnesium sulfate, and evaporated to give p-nitrobenzyl 3-oxo-7-phenoxyacetamidocepham-4-carboxylate (44.5 mg), identical with the product of Example 4.-III (3). Yield: 74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04346218
Source datasetuspto-grants-1982_08
ORD IDord-42b1f2e4aa544ad1a31c83b52e97a96f
Source noteuspto-grants-1982_08