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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455718Generated: October 26, 2026

Valproic Acid → Magnesium;bis(2-propylpentanoate);hydrate

https://huagongshe.com/reaction/1455718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantValproic AcidHCID 3121—
ReactantAcetonitrileHCID 6342—
ReactantMagnesium ValproateHCID 147515—
ReactantMagnesium ethanolateHCID 164963—
SolventEthanolHCID 702—
ProductMagnesium;bis(2-propylpentanoate);hydrateHCID 71439018—

Reaction Steps

A solution of magnesium valproate in absolute ethanol was obtained in the following manner. To a magnetically stirred, clear, colorless solution of valproic acid (31.7 g; 0.22 mol; Sigma Aldrich Chemical Co.) in 200 mL of absolute ethanol was added 11.4 g (0.1 mol) of magnesium ethoxide solid; residual solid was rinsed in with 1 mL of absolute ethanol. Within 30 minutes, a clear, pale yellow solution was obtained; no increase in reaction temperature was observed. Acetonitrile (150 mL) was added to the ethanol solution in portions, and when the addition was complete a white precipitate formed. The reaction mixture was cold to the touch. The slurry was stirred for 15 minutes. The product, magnesium valproate hydrate, was isolated by filtration, washed with fresh acetonitrile, and dried to constant weight. The product, magnesium valproate hydrate, was obtained in 79.8% yield as a white solid, which exhibited an elemental composition identical to that calculated for magnesium valproate hydrate. The product did not melt at temperatures as high as 300° C. The product was not hygroscopic or deliquescent and was stable during storage under ambient conditions. The theoretical valproate content (weight %) of magnesium valproate hydrate is 88.6%; the valproate content found by HPLC analysis was 88.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482486B2
Source datasetuspto-grants-2009_01
ORD IDord-b999b72626de48508ff58376fb6ebcb7
Source noteuspto-grants-2009_01