Diethyl Ether → N-(6-chloro-3-pyridylmethyl)-N-(2,2,2-trifluoroethyl)-N'-methylthiourea

HRID 249529Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 249529
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][NH:9][CH2:10][C:11]([F:14])([F:13])[F:12])=[CH:4][CH:3]=1.[CH3:15][N:16]=[C:17]=[S:18].CCOCC.CCCCCC>C1(C)C=CC=CC=1>[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][N:9]([CH2:10][C:11]([F:14])([F:12])[F:13])[C:17]([NH:16][CH3:15])=[S:18])=[CH:4][CH:3]=1

Komponenten

6

Versuchsvorschrift

In 35 ml of toluene, 3,79 g (0.0169 mole) of N-(6-chloro-3-pyridylmethyl)-N-(2,2,2-trifluoroethyl)amine and 2.46 g of methyl isothiocyanate were stirred for 18 hours under reflux. The toluene was distilled off, and the residue was dissolved in 120 ml of AcOEt, washed with 1N HCl (two times) and aqueous sodium chloride solution in this order and dried over MgSO4. The AcOEt was distilled off to give oil. To this oily product were added Et2O and hexane, followed by cooling to give crystals. After addition of hexane to the mixture, the crystals were collected by filtration and dried to give 2.78 g of N-(6-chloro-3-pyridylmethyl)-N-(2,2,2-trifluoroethyl)-N'-methylthiourea as white crystals.

Aufarbeitung

  1. temperatureunder reflux
  2. distillationThe toluene was distilled off
  3. dissolutionthe residue was dissolved in 120 ml of AcOEt
  4. washwashed with 1N HCl (two times) and aqueous sodium chloride solution in this order
  5. dry with materialdried over MgSO4
  6. distillationThe AcOEt was distilled off
  7. customto give oil
  8. temperatureby cooling
  9. customto give crystals
  10. filtrationthe crystals were collected by filtration
  11. customdried

Quellen und Nachweise

ORD-Eintrag
ord-7f7eca2d63b045f08a7967d80d46fab8
Quelldatensatz
uspto-grants-1993_05
Patentnummer
US05214152

Notizen zur Reaktion

Wird geladen…