HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443913Generated: October 29, 2026
m-Chloroperbenzoic acid → HCID 12810778, compound
https://huagongshe.com/reaction/443913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 12810777 | HCID 12810777 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12810778 | HCID 12810778 | — |
Reaction Steps
A solution of 1-(t-butyldimethylsilyl)-3-(1-hydroxyethyl)-4-(1,1-dimethyl-prop-2-enyl)-azetidin-2-one (3.0 mmol) in dry methylene chloride (30 ml) is cooled to -78° C. (dry ice-acetone) and a stream of ozone is bubbled through until the reaction mixture becomes blue. The ozone flow is then stopped and the reaction is purged by bubbling through nitrogen until the blue color disappears. Solid m-chloroperbenzoic acid (3.0 mmol) is added and the cold bath is removed. When the reaction mixture reaches room temperature, the flask is fitted with a reflux condenser and the mixture is heated at reflux for three days. Removal of solvents in vacuo gives a crude product which is chromatographed on silica gel (2% glacial acetic acid in methylene chloride) to yield 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04262010 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-09392f2bee5a4c9695350fdaac23837a |
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| Source note | uspto-grants-1981_04 |
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