Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 2-Azetidinone | HCID 136721 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | Ruthenium chloride trihydrate | HCID 12090026 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Acetoxy-2-azetidinone | HCID 119981 | 352% |
Reaction Steps
In a Schlenk's tube were charged 710 mg (10 mmole) of azetidin-2-one, 205 mg (2.5 mmole) of anhydrous sodiumacetate, and 130 mg (0.5 mmole, 5 mole %) of ruthenium chloride trihydrate. After thoroughly displacing the atmosphere with oxygen, a balloon filled with oxygen was fitted to the reactor. To the mixture were added 100 ml of ethyl acetate and 5 ml of acetic acid, followed by heating at 40° C. for 30 minutes with stirring. To the reaction mixture was added 1.1 ml (20 mmole) of acetaldehyde all at once while stirring at 40° C., and the reaction was continued for an additional 3 hours. The reaction mixture was poured into 400 ml of a 10% sodium sulfite aqueous solution and extracted twice with 500 ml portions of ethyl acetate. The extract was washed with 200 ml of a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the residue was purified by silica gel column chromatography using a 3:1 (by volume) mixed solvent of n-hexane and ethyl acetate to obtain 1.14 g (8.8 mmole, percent yield: 88%) of 4-acetoxyazetidin-2-one as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05606052 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-6169e7a43fc4459b90d4b8cc4c550b87 |
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| Source note | uspto-grants-1997_02 |
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