Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | 7beta-Phenoxyacetamido-3-hydroxy-3-cephem-4-carboxylic acid p-nitrobenzyl ester | HCID 54716794 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 12784140 | HCID 12784140 | — |
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 recrystallized 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04110533 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-f587f6df83f74cef9e7846a7989e9577 |
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| Source note | uspto-grants-1978_08 |
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