Reacción #1914816

ord-5e418a0388454984873d7145c34719fc

Ecuación de reacción

CCC1(CCl)C(C)OC1C
3-chloromethyl-3-ethyl-2,4-dimethyl-oxetane
Oc1ccc(-c2ccc(O)cc2)cc1
4,4′-bisphenol
[K+].[OH-]
potassium hydroxide
CCC1(COc2ccc(-c3ccc(OCC4(CC)C(C)OC4C)cc3)cc2)C(C)OC1C
4,4′-bis[(2,4-dimethyl-3-ethyl-3-oxetanyl)methoxy]biphenyl

Disolventes

Condiciones de reacción

Temperatura
110°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturato start reflux
  2. 2
    TemperaturaWhile refluxed
  3. 3
    OtroAfter the reaction
  4. 4
    Temperaturathe reaction mixture was cooled to room temperature
  5. 5
    workup.STIRRINGthe resulting mixture was well stirred
  6. 6
    FiltraciónThereafter, deposits were collected by filtration
  7. 7
    LavadoThe resulting deposits were washed with water
  8. 8
    Lavadoby washing with methanol
  9. 9
    OtroSubsequently, drying
  10. 10
    Otrowas obtained

Procedimiento

While stirring, 3-chloromethyl-3-ethyl-2,4-dimethyl-oxetane, 4,4′-bisphenol, and tetrabutylphosphonium bromide were heated to 80° C. An aqueous potassium hydroxide solution was dripped. The resulting mixture was heated to approximately 110° C. to start reflux. While refluxed, the reaction was allowed to proceed over 8 hours. After the reaction, the reaction mixture was cooled to room temperature. Subsequently, pure water was added and the resulting mixture was well stirred. Thereafter, deposits were collected by filtration. The resulting deposits were washed with water, followed by washing with methanol. Subsequently, drying was performed employing a vacuum dryer, whereby a targeted compound was obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07056559B2uspto-grants-2006_06