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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127155Generated: October 23, 2026

Acetone → Potassium Clavulanate

https://huagongshe.com/en/reaction/127155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantLithium phosphateHCID 165867—
Reactant4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, lithium salt (1:1), (2R,3Z,5R)-HCID 23714647—
SolventWaterHCID 962—
ProductPotassium ClavulanateHCID 23665591—

Reaction Steps

Lithium clavulanate (5.15 g, estimated purity 95% pfa, 0.025 moles) was dissolved in 45 mls water and cooled in an ice bath. Tripotassium orthophosphate (10.1 mls of 1 M solution; 1.2 equivs) was added in one lot. The solution was seeded with lithium orthophosphate (1 mg) and acetone (20 ml) added over 1/2 hr. By this time a large quantity of lithium phosphate had separated out and the pH dropped from 8.3 to 7.4. The solution was made up to 100 ml with acetone over 20 minutes and was then made up to 800 mls with acetone over a further 10 minutes. The mixture was stirred with celite (2 gms) and filtered. The clear filtrate was added to acetone (1750 mls) over 1 hr. The white solid was filtered off and washed with acetone (3×50 ml) (being careful not to pull dry on the filter), and dried on a fluid bed dryer to yield potassium clavulanate (5 g, 83.0% pfa, 85% recovery).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255332
Source datasetuspto-grants-1981_03
ORD IDord-0d9965bd1fc5453b8f1b3df09164fb12
Source noteuspto-grants-1981_03