Reacción #1529644

ord-2f87da3be48a451ab93176578c9d3f3e

Disolventes

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA mixture was prepared
  2. 2
    TemperaturaThis suspension was heated
  3. 3
    Temperaturato increase the quantity of precipitate
  4. 4
    OtroThe isopropanol and diethylether were then evaporated off at 30° C.
  5. 5
    Otroa rotary evaporator
  6. 6
    OtroThe organic product formed
  7. 7
    Extracciónwas extracted from the reaction mixture
  8. 8
    ExtracciónThree successive extractions with 10 ml of dichloromethane
  9. 9
    OtroThe organic phase obtained
  10. 10
    Otrowas evaporated
  11. 11
    Otroa rotary evaporator
  12. 12
    OtroThe white solid formed
  13. 13
    Lavadowas washed with dry diethylether
  14. 14
    Filtraciónfiltered 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:

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07658909B2uspto-grants-2010_02