Réaction #47521
ord-8257a5b1b351478a8a78b8d7c1afe0e1
Équation de réaction
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Température
23°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1ConcentrationAfter this time, the mixture was concentrated
- 2workup.ADDITIONthe reaction mixture was diluted with water
- 3AutreThe reaction mixture was acidified with 2N hydrochloric acid, during which time precipitation
- 4AutreThe precipitate was removed by filtration
- 5Lavagewashed with cold water
- 6Autredried in vacuo
Mode opératoire
To a stirred solution of (S)-3-cyclohexyl-2-[4-(2,4-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester (340 mg, 0.001 mol) in tetrahydrofuran-water (3:1, 10 mL) was added lithium hydroxide (106 mg, 0.003 mol). The reaction mixture was stirred at 23° C. for 2 h. After this time, the mixture was concentrated and the reaction mixture was diluted with water. The reaction mixture was acidified with 2N hydrochloric acid, during which time precipitation occurred. The precipitate was removed by filtration, washed with cold water and dried in vacuo to obtain (S)-3-cyclohexyl-2-[4-(2,4-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid (300 mg, 78%) as a light yellow solid.