Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | (4-Hydroxyphenyl)acetamide | HCID 86986 | — |
| Reactant | (-)-Epichlorohydrin | HCID 2734062 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Esatenolol | HCID 175540 | 87% |
Reaction Steps
p-Hydroxyphenylacetamide (1 g) was dissolved in DMF (5 ml) under nitrogen atmosphere and the solution was cooled to 0° C. Cesium fluoride (3.02 g) and sodium iodide (0.1 g) were added thereto and the mixture was stirred for 1 hour. Then (R)-epichlorohydrin (0.62 g, 98.4% e.e.) was added thereto and the mixture was stirred for 30 hours at the same temperature. After the reaction, the reaction mixture was dropped over a period of one hour in isopropylamine (9 g) previously cooled to 10° C. The temperature of the solution was raised to room temperature and stirred for 12 hours. Then the product was treated in the same manner as Example 1 to give 1.53 g of (S)-atenolol (yield 87%, optical purity 98.3% e.e.) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057476 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-685b4a3cf6504058be4d83080647dd21 |
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| Source note | uspto-grants-2000_05 |
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