Reaktion #311835

ord-f4304f6b30ca48fb99fb51f9d84502dd

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture heated
  2. 2
    Temperaturunder reflux for 5 hours
  3. 3
    workup.DISTILLATIONThe acetic acid was distilled off under reduced pressure, and ethyl acetate
  4. 4
    workup.ADDITIONadded to the residue
  5. 5
    WaschenThe organic layer was washed with an aqueous solution of sodium hydrogen carbonate
  6. 6
    Trocknendried over anhydrous magnesium sulfate
  7. 7
    Einengenconcentrated under reduced pressure
  8. 8
    Sonstigeto afford 29.2 g of a crude product
  9. 9
    SonstigeThe product was chromatographed on a column of silica gel

Vorschrift

Alanine ethyl ester hydrochloride (30.8g; 0.2 mole) was dissolved in 100 ml of acetic acid. Acetonylacetone (22.8 g; 0.2 mole) and then 16.4 g (0.2 mole) of sodium acetate were added to the solution, and the mixture heated under reflux for 5 hours. The acetic acid was distilled off under reduced pressure, and ethyl acetate added to the residue. The organic layer was washed with an aqueous solution of sodium hydrogen carbonate, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to afford 29.2 g of a crude product. The product was chromatographed on a column of silica gel using cyclohexane/ethyl acetate (4/1) as an eluent to afford ethyl 2-(2,5-dimethylpyrrol-1-yl)propionate (23.0 g, 0.118 mole, 59.0%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04233309uspto-grants-1980_11