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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3626Generated: October 26, 2026

Sulfuric Acid → Potassium Clavulanate

https://huagongshe.com/reaction/3626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl AcetateHCID 8857—
ReactantClavulanic AcidHCID 5280980—
ReactantPotassium 2-ethylhexanoateHCID 23669619—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductPotassium ClavulanateHCID 2366559173%

Reaction Conditions

Temperature5 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05734048
Source datasetuspto-grants-1998_03
ORD IDord-aa33d2dcc235487b9f952619afa7f8ab
Source noteuspto-grants-1998_03