Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612920Generated: October 26, 2026

Acetic Acid → 2-Azetidinone, 4-(acetyloxy)-3-ethyl-

https://huagongshe.com/reaction/1612920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPeracetic AcidHCID 6585—
ReactantSodium AcetateHCID 517045—
Reactant3-Ethylazetidine-2-oneHCID 19049960—
CatalystTrichloroosmium--water (1/3)HCID 57348105—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-Azetidinone, 4-(acetyloxy)-3-ethyl-HCID 1178843899.3%

Reaction Steps

To a solution prepared by mixing 500 mg (5 mmole) of 3-ethylazetidin-2-one, 415 mg (5 mmole) of anhydrous sodium acetate, 5 ml of acetic acid, and 30 mg (abut 2 mole % based on the amount of 3-ethylazetidin-2-one) of osmium trichloride trihydrate was added dropwise, with stirring , 2.8 g (11 mmole) of a 30% peracetic acid solution in ethyl acetate at room temperature over a period of 2 hours or more. The reaction mixture was further stirred at room temperature for 4 hours, subsequently poured into 80 ml of water, and then extracted thrice with 100 ml of hexane. The extract was dried over anhydrous magnesium sulfate, and the solvent was removed by evaporation under reduced pressure. The residue was separated and purified by silica gel column chromatography (n-hexane/ethyl acetate=1/1 by volume). Thus, 780 mg of 4-acetoxy-3-ethylazetidin-2-one was obtained. The percent yield was 78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05191076
Source datasetuspto-grants-1993_03
ORD IDord-87c16a1c75a1428384c6fc47e701ed4e
Source noteuspto-grants-1993_03