Reaktion #94840

ord-3610284790264e4e93319b0dd2f35d2c

Reaktionsgleichung

S=C=Nc1ccccc1
phenyl isothiocyanate
CCN(CC)CC
triethylamine
Br.CN1CCN(C)C1=N
1,3-dimethyl-2-imino-imidazolidine hydrobromide
CN1CCN(C)C1=NC(=S)Nc1ccccc1
N-(1,3-dimethyl-2-imidazolidinylidene)-N'-phenyl-thiourea

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction mixture is refluxed for 15 hours
  2. 2
    TemperaturAfter cooling
  3. 3
    Waschenit is washed with water
  4. 4
    Trocknendried over sodium sulfate
  5. 5
    Sonstigeevaporated in vacuo

Vorschrift

30.4 g (0.3 mol) of triethylamine are added to a suspension of 58.2 g (0.3 mol) of 1,3-dimethyl-2-imino-imidazolidine hydrobromide in 470 ml of chloroform, at 5°, with stirring. A solution of 40.6 g (0.3 mol) of phenyl isothiocyanate in 235 ml of chloroform is then added dropwise and the reaction mixture is refluxed for 15 hours. After cooling, it is washed with water, dried over sodium sulfate and evaporated in vacuo. Crude N-(1,3-dimethyl-2-imidazolidinylidene)-N'-phenyl-thiourea is obtained and after recrystallisation from ethanol this melts at 195°-196°.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04342764uspto-grants-1982_08