HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → p-Nitrobenzyl 3-oxo-7-phenoxyacetamidocepham-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | p-Nitrobenzyl alpha-[4-mercapto-3-phenoxyacetamido-2-oxoazetidin-1-yl]-alpha-(2-bromo-1-hydroxyethylidene)acetate | HCID 86735550 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | p-Nitrobenzyl 3-oxo-7-phenoxyacetamidocepham-4-carboxylate | HCID 70547786 | 74% |
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 (2ml), 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04160085 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-fc2b8899abb94da0a2c24e0b4678dfd3 |
| Source note | uspto-grants-1979_07 |