関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Atenolol | HCID 2249 | — |
| 反応物 | P-Toluic Acid | HCID 7470 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | Atenolol p-toluate | HCID 86745986 | 50% |
反応手順
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 50 to 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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05223646 |
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| 出典データセット | uspto-grants-1993_06 |
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| ORD ID | ord-90ce5b4de57142c19941570169cf67c1 |
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| 出典メモ | uspto-grants-1993_06 |
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