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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155829Generated: November 1, 2026

Ozone → alpha-[4-Acetylthio-3-phthalimido-2-oxoazetidin-1-yl]-alpha-acetylacetic acid

https://huagongshe.com/reaction/1155829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
Reactantalpha-[4-Acetylthio-3-phthalimido-2-oxoazetidin-1-yl]-alpha-isopropenyl acetic acidHCID 20464336—
SolventMethanolHCID 887—
Productalpha-[4-Acetylthio-3-phthalimido-2-oxoazetidin-1-yl]-alpha-acetylacetic acidHCID 2046440163%

Reaction Steps

To a solution of α-[4-acetylthio-3-phthalimido-2-oxoazetidin-1-yl]-α-isopropenyl acetic acid (100 mg) in methanol (10 ml) at 0° C. is introduced excess ozone. After the gas at the outlet makes a potassium iodide starch paper coloured, the reaction mixture is bubbled with sulfur dioxide gas. The reaction mixture is concentrated, and the obtained residue is dissolved in aqueous solution of sodium hydrogen carbonate, washed with ether, neutralized with hydrochloric acid, and extracted with methylene chloride. The extract solution is washed with water, dried, and evaporated to give α-[4-acetylthio-3-phthalimido-2-oxoazetidin-1-yl]-α-acetyl-acetic acid (64 mg). Yield: 63%. Foam. IR: νmaxCHCl3 1780, 1730, 1680 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04332722
Source datasetuspto-grants-1982_06
ORD IDord-094e371bb8814ed09f41533843c6ec23
Source noteuspto-grants-1982_06