HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464209Generated: October 29, 2026
m-Chloroperbenzoic acid → HCID 131714356, compound
https://huagongshe.com/reaction/464209
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 131714357 | HCID 131714357 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131714356 | HCID 131714356 | 86.1% |
Reaction Steps
To a solution of benzhydryl 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-[2-(3-pyridazinyl)vinyl]-2-cephem-4-carboxylate (syn isomer) (trans isomer) (2.1 g) in methylene chloride (40 ml) was added a solution of 70% m-chloroperbenzoic acid (0.87 g) in methylene chloride (20 ml) at -35° C. with stirring. The reaction mixture was stirred at the same temperature for 20 minutes. The resultant solution was washed with 5% aqueous sodium bicarbonate. The separated organic layer was concentrated under reduced pressure and the residue was triturated in diisopropyl ether to give benzhydryl 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-[2-(3-pyridazinyl)vinyl]-3-cephem-4-carboxylate-1-oxide (syn isomer) (trans isomer) (1.85 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04546101 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-5f729999540042718cab97f5f2a47594 |
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| Source note | uspto-grants-1985_10 |
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