Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 86754829 | HCID 86754829 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54383686 | HCID 54383686 | 64.3% |
Reaction Steps
Ozonised oxygen was bubbled through a solution of p-methoxybenzyl 2-[(3S, 4R)-4-benzylthio-3-bromo-2-oxoazetidin-1-yl]-3-methylbut-2-enoate (2 g, 4 mmol) in dichloromethane (40 ml) at -78° C. and the reaction monitored by infra-red spectroscopy. When the band at 1780 cm-1 had disappeared, methanol (4 ml) together with a trace of sodium methoxide and dimethyl sulfide (1 ml) was added and stirring continued at room temperature for 16 h. The reaction was evaporated and the residue purified by flash chromatography using 1:1 ether:pentane as the eluting solvent. Evaporation of the appropriate fractions gave the product as a colourless oil (0.7 g, 64%). 1H NMR δ (CDCl3) 3.87 (2H, s, SCH2), 4.52 (1H, m, H4), 4.69 (1H, d, H3) 5.85 (1H, bs, NH), 7.18-7.39 (5H, m, Ph--H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05990102 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-e853c40451bf4f3189242e114ed929e7 |
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| Source note | uspto-grants-1999_11 |
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