Reaktion #55406

ord-1250061c6bf742d3bb1159de27181034

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat 25°
  2. 2
    Temperaturthe reaction mixture was refluxed for three hours
  3. 3
    TemperaturThe mixture was cooled
  4. 4
    FiltrationThe precipitate was collected by filtration
  5. 5
    Einengenthe filtrate was concentrated
  6. 6
    workup.ADDITIONbrought to pH 8.5-9 by addition of 10% aqueous sodium hydroxide
  7. 7
    ExtraktionThe resulting suspension was extracted with ethyl acetate
  8. 8
    workup.ADDITIONEthyl acetate was added to the aqueous phase which
  9. 9
    SonstigeThe layers were separated
  10. 10
    Extraktionthe aqueous phase was extracted with ethyl acetate
  11. 11
    Trocknendried (MgSO4)
  12. 12
    Sonstigeevaporated to dryness

Vorschrift

β-Alanine (17.8 g., 0.2 mol.) was added to a solution of 22.4 g. (0.4 mol.) of potassium hydroxide in 500 ml. of water at 25°. Carbon disulfide (12.2 ml., 0.2 mol.) was added and the reaction mixture was refluxed for three hours. The mixture was cooled, 28.4 g. (0.2 mol.) of methyl iodide and 500 ml. of ethanol were added and the resulting mixture was stirred for 30 minutes. The precipitate was collected by filtration, the filtrate was concentrated and the aqueous residue was combined with the solid material and brought to pH 8.5-9 by addition of 10% aqueous sodium hydroxide. The resulting suspension was extracted with ethyl acetate. Ethyl acetate was added to the aqueous phase which was then acidified to pH 1.5 with 6N hydrochloric acid. The layers were separated and the aqueous phase was extracted with ethyl acetate. The ethyl acetate extracts were combined, dried (MgSO4) and evaporated to dryness to give methyl 2-carboxyethyldithiocarbamate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04220644uspto-grants-1980_09