Reacción #1859765

ord-c7d3a48db84e4f808a64d1cf43fca7b7

Ecuación de reacción

C=CCOCCN(C)C
2-(allyloxy)-N,N-dimethylethanamine
CO[SiH](OC)OC
trimethoxysilane
CO[Si](CCCOCCN(C)C)(OC)OC
target compound
Rendimiento 86.0%
CO[Si](CCCOCCN(C)C)(OC)OC
N,N-dimethyl-2-(3-(trimethoxysilyl)propoxy)ethanamine
Rendimiento 86.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroUpon completion of reaction
  2. 2
    Otroafter removing the solvent
  3. 3
    workup.DISTILLATIONthrough distillation under reduced pressure

Procedimiento

After adding toluene (200 mL) to a round-bottom flask containing 2-(allyloxy)-N,N-dimethylethanamine (0.398 mol) and dissolving trimethoxysilane (0.398 mol), a commercially available platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane solution was added and the mixture was stirred for 24 hours. Upon completion of reaction, after removing the solvent through distillation under reduced pressure, 0.342 mol (yield: 86%) of the target compound was obtained by extracting with water and diethyl ether. 1H and 13C NMR spectroscopic data of the purified N,N-dimethyl-2-(3-(trimethoxysilyl)propoxy)ethanamine are as follows.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09249276B2uspto-grants-2016_02