Reaktion #87167

ord-d7d95137c8494587ab35fa3d70aaf3a4

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheated
  2. 2
    Temperaturunder reflux for 7 h
  3. 3
    TemperaturThe mixture was cooled to ambient temperature
  4. 4
    Einengenconcentrated
  5. 5
    SonstigeThe residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=6:1 to 2:1)

Vorschrift

SOCl2 (6.4 g, 54 mmol) was added dropwise to methanol (40 mL) followed by addition of 1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylic acid (5.0 g, 18 mmol) at 0° C. The reaction mixture was stirred at ambient temperature for 1 h and then heated under reflux for 7 h. The mixture was cooled to ambient temperature and concentrated. The residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=6:1 to 2:1) to afford methyl 1-(2,4-dimethoxybenzyl)-5-oxopyrrolidine-3-carboxylate (a mixture of two enantiomers, 4.3 g, 81% yield) as a colorless oil. The two enantiomers were separated by chiral prep-HPLC.

Quelle

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