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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605402Generated: October 31, 2026

m-Chloroperbenzoic acid → Benzhydryl 3-fluoromethyl-7-(2-thienylacetamido)-3-cephem-4-carboxylate-1-oxide

https://huagongshe.com/reaction/1605402

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68132614HCID 68132614—
SolventChloroformHCID 6212—
ProductBenzhydryl 3-fluoromethyl-7-(2-thienylacetamido)-3-cephem-4-carboxylate-1-oxideHCID 68131350—

Reaction Steps

To a solution of 1.04 g of benzhydryl 3-fluoromethyl-7-(2-thienylacetamido)-2-cephem-4-carboxylate in 10 ml of CHCl3 at 0° is added dropwise a solution of 0.35 g of m-chloroperbenzoic acid in 5 ml of CHCl3. The solution is stirred at 0° for 2.5 hours, then diluted with CHCl3 and washed with NaHCO 3, the dried (MgSO4) and evaporated in vacuo. The residue is recrystallized from methanol to yield benzhydryl 3-fluoromethyl-7-(2-thienylacetamido)-3-cephem-4-carboxylate-1-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950329
Source datasetuspto-grants-1976_04
ORD IDord-90a932f6b1114379af9a97dd68aae9b4
Source noteuspto-grants-1976_04