HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612920Generated: October 26, 2026
Acetic Acid → 2-Azetidinone, 4-(acetyloxy)-3-ethyl-
https://huagongshe.com/reaction/1612920
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Ethylazetidine-2-one | HCID 19049960 | — |
| Catalyst | Trichloroosmium--water (1/3) | HCID 57348105 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Azetidinone, 4-(acetyloxy)-3-ethyl- | HCID 11788438 | 99.3% |
Reaction Steps
To a solution prepared by mixing 500 mg (5 mmole) of 3-ethylazetidin-2-one, 415 mg (5 mmole) of anhydrous sodium acetate, 5 ml of acetic acid, and 30 mg (abut 2 mole % based on the amount of 3-ethylazetidin-2-one) of osmium trichloride trihydrate was added dropwise, with stirring , 2.8 g (11 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 further stirred at room temperature for 4 hours, subsequently poured into 80 ml of water, and then extracted thrice with 100 ml of hexane. The extract was dried over anhydrous magnesium sulfate, and the solvent was removed by evaporation under reduced pressure. The residue was separated and purified by silica gel column chromatography (n-hexane/ethyl acetate=1/1 by volume). Thus, 780 mg of 4-acetoxy-3-ethylazetidin-2-one was obtained. The percent yield was 78%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05191076 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-87c16a1c75a1428384c6fc47e701ed4e |
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| Source note | uspto-grants-1993_03 |
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