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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 492225Erstellt: 25. Oktober 2026

Potassium Hydroxide → Levetiracetam

https://huagongshe.com/reaction/492225

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukt4-Chlorobutyryl chlorideHCID 78370—
Edukt(2S)-2-Aminobutanamide hydrochlorideHCID 11961924—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelDichloromethaneHCID 6344—
ProduktLevetiracetamHCID 528458360%

Reaktionsschritte

The compound (−)-(S)-α-ethyl-2-oxo-1-pyrrolidineacetamide is prepared by suspending 50 grams of (S)-2-aminobutyramide hydrochloride in 500 mL of dichloromethane at room temperature, then cooling to temperatures between −5 and 0° C. and adding 81.2 grams of potassium hydroxide and 23.3 grams of tetrabutylammonium bromide at those temperatures. A 66.4 gram amount of 4-chlorobutyryl chloride is added at the same temperatures. After completion of the reaction, solids are removed by filtration, the solution is adjusted to pH 7-7.5 with acetic acid, and dichloromethane is partially evaporated by the application of a vacuum. 150 mL of ethyl acetate are added to precipitate the product, which is isolated by filtration and washed with ethyl acetate and then with acetone; the product has a chiral purity of 99.8 percent by high performance liquid chromatography. The final product is purified by recrystallization from ethyl acetate, giving a yield of 60-65 percent.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07531673B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-c724c900e6574659844ddd9cc0985927
Quellennotizuspto-grants-2009_05