Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 88477147 | HCID 88477147 | — |
| Catalyst | Silver | HCID 23954 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86754829 | HCID 86754829 | 59.1% |
Reaction Steps
A solution of the silver salt of p-methoxybenzyl 2-[(3S, 4R)-4-mercapto-3-bromo-2-oxoazetidin-1-yl]-3-methylbut-2-enoate (10 g, 20 mmol) in dry acetonitrile (100 ml) was treated with benzyl bromide (4 g, 24 mmol) and the resulting mixture refluxed for 30 mins. the reaction was cooled to room temperature, filtered, evaporated to dryness 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 white solid (5.8 g, 59%), mp 70-72° C. 1H NMR δ (CDCl3)1.93 (3H, s, CH3), 2.23 (3H, s, CH3), 3.66 (1H, dd, J=2.9, 17.5 Hz, SCH2), 3.79 (3H, s, OCH3), 4.52 (1H, d, J=1.8 Hz, H3), 4.95 (1H, d, J=1.9 Hz, H4), 5.08 (2H, q, J=12.0 Hz, CO2CH2), 6.84-6.90 (2H, m, 2.6Ph--H), 7.13-7.31 (7H, m, 3,5Ph--H,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-f15e3363a9bb40f1a0ae3a6cbb637892 |
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| Source note | uspto-grants-1999_11 |
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