HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ozone → alpha-[4-Acetylthio-3-phthalimido-2-oxoazetidin-1-yl]-alpha-acetylacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ozone | HCID 24823 | — |
| Reactant | alpha-[4-Acetylthio-3-phthalimido-2-oxoazetidin-1-yl]-alpha-isopropenyl acetic acid | HCID 20464336 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | alpha-[4-Acetylthio-3-phthalimido-2-oxoazetidin-1-yl]-alpha-acetylacetic acid | HCID 20464401 | 63% |
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-acetylacetic acid (64 mg). Yield: 63%. Foam. IR: νmaxCHCl3 1780, 1730, 1680 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04160085 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-9e6ab166918f4f888c3fa8b5bb5338fb |
| Source note | uspto-grants-1979_07 |