Reacción #609429
ord-4c09b81d47124a5fb53fd37dc6c728b5
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.DISTILLATIONdistilled water
- 2workup.ADDITIONis being mixed with a mechanical stirrer
- 3Temperaturato increase the pH to 9.9
- 4workup.ADDITIONThe reaction solution is mixed for one hour
- 5Temperaturathe temperature is increased to 50° C
- 6workup.WAITAfter another hour the reaction solution is
- 7Temperaturato increase the pH to 9.5
- 8workup.ADDITIONAfter four additional hours of mixing at 50° C. the pH is 11.7
- 9Otrois reduced to 20° C.
- 10workup.ADDITIONto mix at room temperature for five hours
- 11TemperaturaThe temperature is increased to 40° C.
- 12Temperaturathe pH is increased to 9.5
- 13Otrothe reaction solution is purged with nitrogen overnight
Procedimiento
In a 2 L reactor system 358.81 g of 3-chloro-1,2-dihydroxypropane (99.3%, 3.22 moles) is added to 734.20 g distilled water. The solution is heated to 30° C. and 496.29 g dimethyloctylamine (98.5%, 3.11 moles) is added over 60 minutes while the reaction solution is being mixed with a mechanical stirrer. The pH is 8.9 and 3.83 g sodium hydroxide (50%) is added to increase the pH to 9.9. The reaction solution is mixed for one hour and then the temperature is increased to 50° C. After another hour the reaction solution is a “milky white” and the pH is 8.3. 19.6 g sodium hydroxide (50%) is added to increase the pH to 9.5. After four additional hours of mixing at 50° C. the pH is 11.7; 11.97 g concentrated hydrochloric acid is added to decrease the pH to 9.0. Thirty minutes later 3.30 g of concentrated hydrochloric acid is added to decrease the pH to 8.9. The solution is allowed to stir for 16 hours at 50° C. The reaction solution pH is 10.7 and 2.58 g concentrated hydrochloric acid is added to reduce the pH to 8.0. The temperature is reduced to 20° C. and 24.23 g trimethylamine (43.6%) is added and allowed to mix at room temperature for five hours. The temperature is increased to 40° C. and the pH is increased to 9.5 and the reaction solution is purged with nitrogen overnight. The solution is pH adjusted to 6.5 with concentrated hydrochloric acid. The isolated product has the following structure: