Reacción #68739

ord-175e34ccb8e8436d845b25e2912b3ff5

Disolventes

Condiciones de reacción

Temperatura
82°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA 100 ml 3-neck flask was fitted with an overhead stirrer
  2. 2
    Extracciónextracted with aqueous sodium hydroxide
  3. 3
    Lavadowashed three times with water
  4. 4
    OtroSolvent was removed by rotary evaporation
  5. 5
    OtroSome polymer precipitated
  6. 6
    Otrowas removed
  7. 7
    OtroSolvent was removed by rotary evaporation
  8. 8
    Filtraciónfiltered
  9. 9
    OtroSolvent was removed by rotary evaporation
  10. 10
    OtroRemaining volatiles were removed by vacuum distillation (29″, 196° C.)
  11. 11
    Otroto yield a viscous, dark yellow liquid

Procedimiento

A 100 ml 3-neck flask was fitted with an overhead stirrer, a thermocouple and a nitrogen inlet. The flask was charged with N,N,N′-tricyclohexyl-para-phenylenediamine (27.1 g), methyl acrylate (150 ml) and glacial acetic acid (10 ml). The reaction was stirred at 82° C. until complete. The reaction mass was taken up in xylenes, extracted with aqueous sodium hydroxide and washed three times with water. Solvent was removed by rotary evaporation. The reaction mass was taken up in hexanes. Some polymer precipitated and was removed. Solvent was removed by rotary evaporation. The product was taken up in xylenes and filtered. Solvent was removed by rotary evaporation. Remaining volatiles were removed by vacuum distillation (29″, 196° C.) to yield a viscous, dark yellow liquid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08530397B2uspto-grants-2013_09