参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 四氧化硫 | HCID 1118 | — |
| 反应物 | 乙酸乙酯 | HCID 8857 | — |
| 反应物 | 克拉维酸 | HCID 5280980 | — |
| 反应物 | Potassium 2-ethylhexanoate | HCID 23669619 | — |
| 溶剂 | 4-甲基-2-戊酮 | HCID 7909 | — |
| 产物 | 克拉维酸钾 | HCID 23665591 | 73% |
反应步骤
100 ml of the solvent mixture of ethyl acetate and methyl isobutyl ketone (4:1) already cooled to 5° C. was added to 100 ml of aqueous solution containing clavulanic acid (12 mg/ml). While agitating the mixture, 50% sulfuric acid was slowly added in order to control pH at 1.5. After extracting the said mixture, the extracts are separated. The remaining aqueous solution was further extracted with 100 ml of the solvent mixture three times. Anhydrous magnesium sulfate (10 g) and activated carbon(10 g) were added to the combined extract, and the resultant mixture was agitated at 5° C. for 30 minutes. The mixture was suction-filtered through a filter, and the remaining material was washed with 50 ml of methyl isobutyl ketone. A solution of potassium 2-ethylhexanoate (1.5 equivalent) dissolved in methyl isobutyl ketone was slowly added to the said extract, and the mixture was agitated at 5° C. for 2 hours. The crystalline product was filtered and slurried with acetone at the same temperature for 2 hours. The crystalline was dried in a vacuum desiccator (30° C.) for about 5 hours to obtain 1.07 g of potassium clavulanate (yield: 73%).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US05734048 |
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| 来源数据集 | uspto-grants-1998_03 |
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| ORD ID | ord-aa33d2dcc235487b9f952619afa7f8ab |
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| 来源说明 | uspto-grants-1998_03 |
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