Reaktion #1176550

ord-4fff79cbbbc643ce85078d63c0701996

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder cooling with a Dry Ice/methanol bath
  2. 2
    Sonstigethe reaction
  3. 3
    workup.STIRRINGstirred for an additional 1 hour
  4. 4
    SonstigeThe solvent was removed in vacuo
  5. 5
    workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
  6. 6
    WaschenThe solution was washed twice with a saturated aqueous solution of sodium bicarbonate
  7. 7
    TrocknenAfter drying over unhydrous sodium sulfate
  8. 8
    Sonstigethe solvent was evaporated in vacuo
  9. 9
    Sonstigeto produce a pale yellow crystal
  10. 10
    Sonstigein an amount of 5.29 g (yield, 98%)

Vorschrift

Thionyl chloride (3.1 ml, 42.5 mmol) was added slowly to methanol (30 ml) with stirring under cooling with a Dry Ice/methanol bath. After allowing the reaction to warm to room temperature, 3-(4-methoxyphenyl)propionic acid (5 g, 27.7 mmol) was added and stirred for an additional 1 hour. The solvent was removed in vacuo and the residue was dissolved in ethyl acetate. The solution was washed twice with a saturated aqueous solution of sodium bicarbonate, then once with a saturated aqueous solution of sodium chloride. After drying over unhydrous sodium sulfate, the solvent was evaporated in vacuo to produce a pale yellow crystal in an amount of 5.29 g (yield, 98%). Rf1 : 0.83

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04965405uspto-grants-1990_10