Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ketoprofen | HCID 3825 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Cinchonidine | HCID 101744 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (S)-(-)-Ketoprofen cinchonidine | HCID 131717639 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05162576 |
|---|
| Quelldatensatz | uspto-grants-1992_11 |
|---|
| ORD ID | ord-59bbdc689ce24ee88b2bfe0a985a3868 |
|---|
| Quellennotiz | uspto-grants-1992_11 |
|---|