Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Azetidinone | HCID 136721 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | Ruthenium trichloride | HCID 61850 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Acetoxy-2-azetidinone | HCID 119981 | 71.3% |
Reaction Steps
0.71 g of azetidine-2-one and 0.82 g of anhydrous sodium acetate were suspended in 20 ml of acetonitrile and cooled to -5°, to which 10 ml of acetonitrile containing 0.26 g of ruthenium trichloride.3H2O was added. 3.8 ml of acetic acid containing 40% peracetic acid was carefully dropped thereto so as to maintain the temperature not higher than 0° C., then continuously stirred at 0° C. for 30 minutes. The solvent was distilled off under reduced pressure at a temperature not higher than 40° C., and subjected to silica gel chromatography (eluent: n-hexane: ethyl acetate=1:1) for purification to obtain 0.92 g of the title compound (yield 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05204460 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-d22715f73ace46d5a735eb4fe3e5423c |
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| Source note | uspto-grants-1993_04 |
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