Reaktion #87168

ord-ba39b1f2e5784110a13983a6297909ce

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeTHF was removed
  2. 2
    Waschenthe remaining aqueous solution was washed with diethyl ether (50 mL×2)
  3. 3
    Extraktionthe resulting mixture was extracted with DCM (40 ml×3)
  4. 4
    WaschenThe combined extracts were washed with water (100 mL×3) and brine (100 mL×1)
  5. 5
    Trocknendried over anhydrous sodium sulfate
  6. 6
    Einengenconcentrated

Vorschrift

LiOH (1.36 g, 32.5 mmol) was added to a solution of (R)-methyl 1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylate (3.18 g, 10.9 mmol) in THF/H2O (1:1, 40 mL) at 0° C. and the reaction mixture was stirred for 1 h. THF was removed and the remaining aqueous solution was washed with diethyl ether (50 mL×2). The aqueous phase was adjusted to pH=5 with 3 N aqueous HCl and the resulting mixture was extracted with DCM (40 ml×3). The combined extracts were washed with water (100 mL×3) and brine (100 mL×1), dried over anhydrous sodium sulfate and concentrated to afford compound (R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylic acid (2.76 g, 88% yield) as a colorless solid. (S)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylic acid was prepared using the same method.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09434761B2uspto-grants-2016_09