Reacción #1529644
ord-2f87da3be48a451ab93176578c9d3f3e
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroA mixture was prepared
- 2TemperaturaThis suspension was heated
- 3Temperaturato increase the quantity of precipitate
- 4OtroThe isopropanol and diethylether were then evaporated off at 30° C.
- 5Otroa rotary evaporator
- 6OtroThe organic product formed
- 7Extracciónwas extracted from the reaction mixture
- 8ExtracciónThree successive extractions with 10 ml of dichloromethane
- 9OtroThe organic phase obtained
- 10Otrowas evaporated
- 11Otroa rotary evaporator
- 12OtroThe white solid formed
- 13Lavadowas washed with dry diethylether
- 14Filtraciónfiltered over a nylon membrane (diameter=0.2 μm)
Procedimiento
A mixture was prepared containing 1 g (0.77×10−2 moles) of N,N,3,3-tetramethylbutylamine (Aldrich) and 1.917 g (1.16×10−2 moles) of 1-bromo-3,3-dimethylbutane (Prolabo) and about 4 ml of isopropanol. Next, 1.23 g (1.16×10−2 mole) of sodium carbonate was added. This suspension was heated under reflux for 2 days at a temperature of 100° C. A white solid appeared and after this time, about 5 ml of diethylether was added to the reaction mixture to increase the quantity of precipitate. The isopropanol and diethylether were then evaporated off at 30° C. using a rotary evaporator. The organic product formed was extracted from the reaction mixture using dichloromethane. Three successive extractions with 10 ml of dichloromethane were carried out. The organic phase obtained was evaporated using a rotary evaporator. The white solid formed was washed with dry diethylether and filtered over a nylon membrane (diameter=0.2 μm). 0.8 g (0.27×10−2 moles) of N,N-dimethyl-N,N-di(3,3-dimethylbutyl)ammonium bromide (DMDMBA-Br) was obtained. The nature of the species obtained was verified by proton nuclear magnetic resonance; the results of this analysis are given below: