3-chloro-2-oxopropyl N-(2,3,4-trifluorophenyl)dithiocarbamate → 2(3H)-Thiazolethione, 4-(chloromethyl)-3-(2,3,4-trifluorophenyl)-

HRID 373913Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 373913
[F:1][C:2]1[C:7]([F:8])=[C:6]([F:9])[CH:5]=[CH:4][C:3]=1[NH:10][C:11](=[S:18])[S:12][CH2:13][C:14](=O)[CH2:15][Cl:16].[H][H]>>[Cl:16][CH2:15][C:14]1[N:10]([C:3]2[CH:4]=[CH:5][C:6]([F:9])=[C:7]([F:8])[C:2]=2[F:1])[C:11](=[S:18])[S:12][CH:13]=1

Komponenten

3

Edukt 2

HCID 100869643-chloro-2-oxopropyl N-(2,3,4-trifluorophenyl)dithiocarbamateHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 41903592(3H)-Thiazolethione, 4-(chloromethyl)-3-(2,3,4-trifluorophenyl)-

Versuchsvorschrift

3-Chloro-2-oxopropyl N-(2,3,4-trifluorophenyl)-dithiocarbamate (4.0 g) is added to 30% hydrogen chloridemethanol solution (15 ml), and the mixture is refluxed for 3 hours. The solvent is distilled off under reduced pressure, and cold water is added to the residue and the mixture is extracted with chloroform. The extract is washed with saline solution, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue is recrystallized from cyclohexane to give the title compound (2.6 9) as pale yellow crystals.

Aufarbeitung

  1. temperaturethe mixture is refluxed for 3 hours
  2. distillationThe solvent is distilled off under reduced pressure, and cold water
  3. additionis added to the residue
  4. extractionthe mixture is extracted with chloroform
  5. washThe extract is washed with saline solution
  6. dry with materialdried over anhydrous sodium sulfate
  7. distillationdistilled under reduced pressure
  8. customto remove the solvent
  9. customThe residue is recrystallized from cyclohexane

Quellen und Nachweise

ORD-Eintrag
ord-3ba03564df7e489faad5c9f72aa8a510
Quelldatensatz
uspto-grants-1992_11
Patentnummer
US05166203

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