تفاعل #3722

ord-aa33d2dcc235487b9f952619afa7f8ab

ظروف التفاعل

درجة الحرارة
5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05734048uspto-grants-1998_03