تفاعل #3722
ord-aa33d2dcc235487b9f952619afa7f8ab
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المعالجة
- 1workup.ADDITIONwas slowly added in order
- 2استخلاصAfter extracting the said mixture
- 3أخرىthe extracts are separated
- 4استخلاصThe remaining aqueous solution was further extracted with 100 ml of the solvent mixture three times
- 5workup.ADDITIONAnhydrous magnesium sulfate (10 g) and activated carbon(10 g) were added to the
- 6استخلاصcombined extract
- 7ترشيحThe mixture was suction-filtered through a filter
- 8غسيلthe remaining material was washed with 50 ml of methyl isobutyl ketone
- 9workup.ADDITIONwas slowly added to the
- 10استخلاصsaid extract
- 11workup.STIRRINGthe mixture was agitated at 5° C. for 2 hours
- 12ترشيحThe crystalline product was filtered
- 13workup.WAITslurried with acetone at the same temperature for 2 hours
- 14أخرىThe crystalline was dried in a vacuum desiccator (30° C.) for about 5 hours
الإجراء التجريبي
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%).