Reacción #944022

ord-b1f4b954edb34e5c9a6451808d73c45e

Ecuación de reacción

CCCC=O
butyraldehyde
CC(C)NC(C)C
diisopropylamine
CCC=CN(C(C)C)C(C)C
title compound
Rendimiento 65.0%
CCC=CN(C(C)C)C(C)C
1-(N,N-Diisopropylamino)-1-butene
Rendimiento 65.0%

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture was heated
  2. 2
    Temperaturaunder reflux
  3. 3
    Otrowhile removing the water
  4. 4
    Otroproduced, until the production of water
  5. 5
    Otro(about 15 hours)
  6. 6
    OtroThe solvent was then removed by distillation under reduced pressure
  7. 7
    workup.DISTILLATIONthe residue was distilled under atmospheric pressure
  8. 8
    Otroof from 140 to 160° C.
  9. 9
    Otrowere collected

Procedimiento

6.25 ml (69.3 mmol) of butyraldehyde and 19.44 ml (139 mmol) of diisopropylamine were dissolved in 30 ml of benzene, and the mixture was heated under reflux, while removing the water produced, until the production of water stopped (about 15 hours). The solvent was then removed by distillation under reduced pressure, and the residue was distilled under atmospheric pressure. Those fractions of the distillate having a boiling point of from 140 to 160° C. were collected, to give 6.95 g of the title compound as a pale yellow oily substance (yield 65%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE039420E1uspto-grants-2006_12