Reacción #47531
ord-d25a97f750f8449cb79c720ec04a1ce9
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
23°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ConcentraciónAfter this time, the mixture was concentrated
- 2workup.ADDITIONthe reaction mixture was diluted with water
- 3OtroThe reaction mixture was acidified with 2N hydrochloric acid, during which time precipitation
- 4OtroThe precipitate was removed by filtration
- 5Lavadowashed with cold water
- 6Otrodried in vacuo
Procedimiento
To a stirred solution of (S)-3-cyclohexyl-2-[4-(2,3-dimethyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester (850 mg, 0.002 mol) in tetrahydrofuran-water (3:1, 10 mL) was added lithium hydroxide (287 mg, 0.012 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-(2,3-dimethyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid (720 mg, 88%) as an off-white solid.