Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Atenolol | HCID 2249 | — |
| Edukt | P-Toluic Acid | HCID 7470 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | Atenolol p-toluate | HCID 86745986 | — |
Reaktionsschritte
The atenolol having low optical purity (1 mole) and p-toluic acid (1 mole) are dissolved in acetone (5 to 50 liters) with heating and the mixture is stirred at 0° to 15° C. for 5 to 24 hours. The precipitated crystals are removed by filtration, and the mother liquor is concentrated to give an optically active atenolol p-toluate with having higher optical purity, for example a salt having an optical purity of 98% ee or more from a salt having an optical purity of 91% ee in a yield of 50to 80%. In this method, when benzoic acid is used instead of p-toluic acid and chloroform is used instead of acetone, similar result is obtained. When p-t-butylbenzoic acid is used instead of p-toluic acid in the above method, the produced salt is hardly soluble in a solvent, and hence, it is necessary to use a solvent having higher solubility such as ethanol or 2-propanol instead of acetone.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05130482 |
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| Quelldatensatz | uspto-grants-1992_07 |
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| ORD ID | ord-689485422967476a86cb81a82ba04ac4 |
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| Quellennotiz | uspto-grants-1992_07 |
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