1,1,2,2-Tetrachloroethylsulfenyl chloride → N-isopropyl-N-(trichlorovinylthio)-chloromethanesulfonamide
Reaktionsgleichung
[CH:1]([NH:4][S:5]([CH2:8][Cl:9])(=[O:7])=[O:6])([CH3:3])[CH3:2].[Cl:10][C:11](Cl)([S:15]Cl)[CH:12]([Cl:14])[Cl:13]>C(N(CC)CC)C>[CH:1]([N:4]([S:15][C:11]([Cl:10])=[C:12]([Cl:14])[Cl:13])[S:5]([CH2:8][Cl:9])(=[O:7])=[O:6])([CH3:3])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A 32.3 g (0.32 mol) sample of triethylamine was added dropwise to a cooled (0° C.) solution of 50 g (0.29 mol) N-isopropyl chloromethanesulfonamide and 70 g (0.29 mol) 1,1,2,2-tetrachloroethylsulfenyl chloride. After the addition was completed, the reaction was stirred at ambient temperature for 30 minutes and then under reflux for 3 hours. The reaction mixture was then cooled, washed with water, dried over magnesium sulfate and evaporated under reduced pressure to give the N-isopropyl-N-(trichlorovinylthio)-chloromethanesulfonamide product, which after crystallization from pet. ether melted at 71°-73° C. The product is reported as Compound 1.