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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 373356Erstellt: 24. Oktober 2026

Ketoprofen → (S)-(-)-Ketoprofen cinchonidine

https://huagongshe.com/de/reaction/373356

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktKetoprofenHCID 3825—
EduktEthyl AcetateHCID 8857—
EduktCinchonidineHCID 101744—
LösungsmittelMethanolHCID 887—
Produkt(S)-(-)-Ketoprofen cinchonidineHCID 13171763931%

Reaktionsbedingungen

Temperatur35 °C

Reaktionsschritte

Cinchonidine (155 g; 0.53 mol) was added to a solution of 115g (0.59 mol) of racemic ketoprofen and 2.8 L of ethyl acetate under vigorous stirring at 50°-60° C. The mixture was diluted with 280 mL of methanol, cooled to 35° C., then seeded with 98% enantiomerically pure S-salt to induce crystallization. After stirring at room temperature for 16 h and 0° C. for 5-6 h, the precipitated diastereomeric salt was filtered under vacuum, washed three times with ethyl acetate and three times with ether, and then dried under vacuum for 16 h [Yield: 127 g (or 44%); enantiomeric purity: 86% S]. One recrystallization from 1.7 L of ethyl acetate/methanol (10:1) afforded 88 g (31% yield) salt of 97% enantiomerically pure S-ketoprofen.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05162576
Quelldatensatzuspto-grants-1992_11
ORD IDord-59bbdc689ce24ee88b2bfe0a985a3868
Quellennotizuspto-grants-1992_11