Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127159Generated: October 23, 2026

Acetone → Potassium Clavulanate

https://huagongshe.com/en/reaction/127159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantIsopropanolHCID 3776—
ReactantPotassium Phosphate, TribasicHCID 62657—
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 (7.15 g, estimated purity 68% pfa; 0.025 M) was stirred in water (45 mls) and about 200 mg insoluble material filtered off. The filtrate (dark brown) was chilled in an ice bath and the potassium phosphate (10.1 mls of 1 M solution; 1.2 equivalents) added in one lot. Isopropanol (32 mls) was added over 1/2 hr by which time some gummy material separated out. The mixture was made up to 100 ml with acetone over 1/4 hr and transferred to another vessel leaving behind a pale gummy deposit. The decanted liquor was then made up to 800 ml with acetone causing the precipitation of highly coloured (brown) gummy material which was separated off via filtration with celite (4 gm). The clear pale yellow solution was then added to acetone (1750 ml) over 1 hr, stirring vigorously and the mixture was then filtered to afford a pale yellow solid which was washed with acetone (3×50 ml) and dried on a fluid bed dryer to yield potassium clavulanate (2 g, 81.2% pfa, 33% recovery).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255332
Source datasetuspto-grants-1981_03
ORD IDord-a3a789e875744401bdd80f488f9bf49c
Source noteuspto-grants-1981_03