HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615115Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 20429039, compound
https://huagongshe.com/reaction/615115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 14230826 | HCID 14230826 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20429039 | HCID 20429039 | 91.2% |
Reaction Steps
To a solution of benzyl 7-phenoxyacetamido-8-oxo-3-trifluoromethanesulfonyl-5-thia-1,3-diazabicyclo[4,2,0]octane-2-carboxylate (1.172 g.) in methylene chloride (10 ml.) was added dropwise a solution of m-chloroperbenzoic acid (430 mg.) in methylene chloride (6 ml.) at 0° C. with stirring over a period of 20 minutes, and the mixture was stirred for an additional 15 minutes. The mixture was diluted with methylene chloride and washed with a chilled dilute aqueous solution of sodium bicarbonate and a mixture of a dilute aqueous solution of sodium chloride and an aqueous solution of sodium bicarbonate. Drying over magnesium sulfate and removal of the solent left an amorphous solid (1.2 g.), which was chromatographed on silica gel (17 g.) with methylene chloride and then a mixed solvent of methylene chloride and ethyl acetate as an eluent to give an amorphous solid (1.10 g.) of benzyl 7-phenoxyacetamido-8-oxo-3-trifluoromethanesulfonyl-5-thia-1,3-diazabicyclo[4,2,0]octane-2-carboxylate-5-oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04497738 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-e74b26bac90e4bd7b4232cfc1578de70 |
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| Source note | uspto-grants-1985_02 |
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