HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-Acetoxy-2-azetidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | 2-Azetidinone | HCID 136721 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | Trichloroosmium--water (1/3) | HCID 57348105 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Acetoxy-2-azetidinone | HCID 119981 | 78.6% |
Reaction Steps
To a mixture of 200 mg (2.8 mmole) of azetidin-2-one, 230 mg (2.8 mmole) of anhydrous sodium acetate, 2 ml of acetic acid, and 17 mg (2 mole % based on the amount of azetidin-2-one) of osmium trichloride trihydrate was added dropwise, with stirring, 1.56 g (6.2 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 poured into 50 ml of water and extracted with n-hexane. The extract was separated and purified by silica gel column chromatography (n-hexane/ethyl acetate=1/1 by volume). Thus, 280 mg (2.2 mmole, percent yield: 78%) of 4-acetoxyazetidin-2-one in a colorless oily state was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05191076 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-de9a6296fadd4eaebc11e1bdd66e2e6b |
| Source note | uspto-grants-1993_03 |