Réaction #51243

ord-a33fe86201f24b20b09fad2d95879b46

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe reaction was partitioned between methylene chloride (150 mL) and aqueous sodium bicarbonate solution (150 mL)
  2. 2
    Autrethe phases were separated
  3. 3
    SéchageThe organic phase was dried (K2CO3)
  4. 4
    Filtrationfiltered
  5. 5
    AutreThe filtrate was evaporated under reduced pressure

Mode opératoire

To a solution of (5R)-5-(hydroxymethyl)pyrrolidin-2-one (Aldrich, 8.86 g, 77 mmol) in 70 mL of chloroform at room temperature under an argon atmosphere was added ethyl vinyl ether (10.4 mL, 108 mmol) and catalytic anhydrous trifluoroacetic acid (0.2 mL). After stirring for 3 hours, the reaction was partitioned between methylene chloride (150 mL) and aqueous sodium bicarbonate solution (150 mL) and the phases were separated. The organic phase was dried (K2CO3) and filtered. The filtrate was evaporated under reduced pressure to give 14.7 g of the (5R)-5-(1-ethoxyethoxymethyl)pyrrolidin-2-one.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06849657B2uspto-grants-2005_02