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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090294Generated: October 25, 2026

Peracetic Acid → 4-Acetoxy-2-azetidinone

https://huagongshe.com/reaction/1090294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPeracetic AcidHCID 6585—
ReactantSodium AcetateHCID 517045—
Reactant4-Oxoazetidine-2-carboxylic acidHCID 3488064—
CatalystHCID 178503044HCID 178503044—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product4-Acetoxy-2-azetidinoneHCID 119981109.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.3 g of 4-hydroxycarbonylazetidine-2-one, 0.43 g of anhydrous sodium acetate and 100 mg of 5% ruthenium-carbon were suspended in a mixture of 12 ml of methylene chloride and 4 ml of acetic acid and cooled to -3° C., to which 1.1 ml of acetic acid solution containing 40% peracetic acid was carefully dropped, subjected to stirring at 0° C. for 1 hour. The catalyst was separated by suction filtration, then solvent was distilled off under reduced pressure. 20 ml of n-hexane was added thereto. Undissolved matter was filtered off, the filtrate was concentrated under reduced pressure to obtain 0.37 g of the title compound (yield: 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081239
Source datasetuspto-grants-1992_01
ORD IDord-add079eafdf4413e96b6c3205e1426cc
Source noteuspto-grants-1992_01