Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 131716916 | HCID 131716916 | — |
| Catalyst | Cupric acetate monohydrate | HCID 165397 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 77316455 | HCID 77316455 | 77.6% |
Reaction Steps
A mixture of 351 mg (1 mmol) of (1'R, 3S, 4R)-3-(1'-tert-butyldimethylsililoxy)ethyl-4-p-methylphenylthio-2-azetidinone and 100 mg (0.5 mmol) of copper (II) acetate monohydrate in 2 ml of acetic acid was heated at 110° C. for 5 minutes with stirring. The reaction mixture was diluted with ether and the insoluble materials were filtered off. The filtrate was washed with saturated sodium bicarbonate solution and then water, dried, and concentrated to produce 223 mg (yield: 77.6%) of the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05026844 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-856b26e674d1441ebe0e56a58d944b03 |
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| Source note | uspto-grants-1991_06 |
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