Reacción #2370332

ord-1aa44e8d6c6f4c469c97eb084bef1dee

Ecuación de reacción

C#Cc1cccc(OC(F)(F)C(F)OC(F)(F)C(F)(OC(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F)c1
1-ethynyl-3-(1,1,2-trifluoro-2-(1,1,2,3,3,3-hexafluoro-2-(perfluoropropoxy)propoxy)ethoxy)benzene
CC(=O)c1ccc(O)cc1
1-(4-hydroxyphenyl)ethanone
O=C([O-])[O-].[K+].[K+]
Potassium carbonate
FC(F)=C(F)OC(F)(F)C(F)(F)C(F)(F)F
1,1,1,2,2,3,3-heptafluoro-3-((1,2,2-trifluorovinyl)oxy)propane
CC(=O)c1ccc(OC(F)(F)C(F)OC(F)(F)C(F)(F)C(F)(F)F)cc1
1-(4-(1,1,2-trifluoro-2-(perfluoropropoxy)ethoxy)phenyl)ethanone

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroequipped with a stirrer
  2. 2
    Otrothe reaction was placed in an oil bath
  3. 3
    Temperaturaheated to
  4. 4
    Temperaturaa gentle reflux for 5.5 hours

Procedimiento

In the dry box, tetrahydrofuran (50 mL) and 1-(4-hydroxyphenyl)ethanone (0.68 g, 0.005 mol) were added to a round bottom flask equipped with a stirrer. Potassium carbonate (0.175 g, 0.00126 mol) was then added to the flask. 1,1,1,2,2,3,3-heptafluoro-3-((1,2,2-trifluorovinyl)oxy)propane (1.99 g, 0.0075 mol) was then added via the addition funnel and the reaction was placed in an oil bath and heated to a gentle reflux for 5.5 hours. The content was analyzed by proton NMR and shown to be 1-ethynyl-3-(1,1,2-trifluoro-2-(1,1,2,3,3,3-hexafluoro-2-(perfluoropropoxy)propoxy)ethoxy)benzene.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09145356B2uspto-grants-2015_09