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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252310Generated: November 3, 2026

m-Chloroperbenzoic acid → HCID 141551045, compound

https://huagongshe.com/reaction/1252310

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 88521895HCID 88521895—
SolventBenzeneHCID 241—
ProductHCID 141551045HCID 14155104593%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742053
Source datasetuspto-grants-1988_05
ORD IDord-e5ee3938e11a4d349d0842b6cdb5a714
Source noteuspto-grants-1988_05