HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252310Generated: November 3, 2026
m-Chloroperbenzoic acid → HCID 141551045, compound
https://huagongshe.com/reaction/1252310
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 88521895 | HCID 88521895 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 141551045 | HCID 141551045 | 93% |
Reaction Steps
4.0 g (4.7 mmol) of benzhydryl 7-[(Z)-2-ethoxyimino-2-(2-tritylaminothiazol-4-yl)acetamido]-3-chloromethyl-3-cephem-4-carboxylate was dissolved in 40 ml of benzene, and 1.0 g (5.8 mmol) of m-chloroperbenzoic acid was added under cooling with ice. The mixture was stirred at room temperature for 40 minutes. The reaction solution was poured into ice water, and extracted with ethyl acetate. The extract solution was washed with a 5% acid sodium bisulfite aqueous solution and with a saturated sodium chloride aqueous solution, then dried over anhydrous sodium sulfate and concentrated under reduced pressure. The oily residue was solidified by an addition of n-hexane, collected by filtration and dried to obtain 3.8 g (yield: 93%) of a powder of the above identified compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04742053 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-e5ee3938e11a4d349d0842b6cdb5a714 |
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| Source note | uspto-grants-1988_05 |
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