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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286285Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 131712702, compound

https://huagongshe.com/reaction/2286285

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 131712703HCID 131712703—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131712702HCID 13171270279.7%

Reaction Steps

To a solution of benzhydryl 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-(1-imidazolyl)carbonyloxymethyl-3-cephem-4-carboxylate (syn isomer)(13.5 g) in tetrahydrofuran (200 ml) was added m-chloroperbenzoic acid (5.8 g) with stirring under ice-cooling, followed by stirring for an hour at 5° C. The reaction mixture was evaporated and the residue was pulverized in diethyl ether, collected by filtration, washed with ethyl acetate and diethyl ether and then dried to give benzhydryl 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-(1-imidazolyl)carbonyloxymethyl-3-cephem-4-carboxylate-1-oxide (syn isomer)(11.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04327093
Source datasetuspto-grants-1982_04
ORD IDord-286ac80c07f444b0ab3e3cf600b65d9a
Source noteuspto-grants-1982_04