Reaction #47540

ord-505d1444decd43d4b77172dceea94ae5

Conditions

Temperature
23°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    ConcentrationAfter this time, the mixture was concentrated
  2. 2
    workup.ADDITIONthe reaction mixture was diluted with water
  3. 3
    OtherThe reaction mixture was acidified with 2N hydrochloric acid, during which time precipitation
  4. 4
    OtherThe precipitate was removed by filtration
  5. 5
    Washwashed with cold water
  6. 6
    Otherdried in vacuo

Procedure

To a stirred solution of (S)-3-cyclohexyl-2-[4-(3-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester (1.10 g, 0.003 mol) in tetrahydrofuran-water (3:1, 10 mL) was added lithium hydroxide (382 mg, 0.016 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-(3-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid (920 gm, 87%) as an off-white solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741327B2uspto-grants-2010_06