Reacción #8657

ord-8f56d2638ebd4d958343cc0fd1c539ea

Condiciones de reacción

Temperatura
90°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe resulting colorless solution was deoxygenated
  2. 2
    Otroby gently bubbling a stream of N2 through the stirring solution for 15 minutes
  3. 3
    workup.ADDITIONwas then added to the refluxing mixture over 10 minutes
  4. 4
    TemperaturaThe polymerization was then refluxed
  5. 5
    Temperaturacooled to room temperature
  6. 6
    Filtraciónfiltered
  7. 7
    Otrodried
  8. 8
    workup.DISSOLUTIONre-dissolved in 70 mL of tetrahydrofuran
  9. 9
    Otroprecipitated into 800 mL of hexanes
  10. 10
    Filtraciónfiltered
  11. 11
    Lavadowashed well with hexanes
  12. 12
    Otrodried in a vacuum oven at 40° C. for 24 hours

Procedimiento

2-Methyladamantanyl methacrylate (14.21 g, 0.061 mol), methacrylonitrile (3.05 g, 0.045 mol), and alpha-butyrolactone methacrylate (7.74 g, 0.045 mol) were dissolved in 66 mL of tetrahydrofuran. The resulting colorless solution was deoxygenated by gently bubbling a stream of N2 through the stirring solution for 15 minutes, placed under N2, and heated to 90° C. (oil bath temperature). VAZO67 (0.58 g, 0.0030 mol) dissolved in 7 ml of tetrahydrofuran, was then added to the refluxing mixture over 10 minutes. The polymerization was then refluxed with stirring for 20 hours and cooled to room temperature. The polymer was isolated by precipitation into 800 mL of hexanes, filtered, dried, re-dissolved in 70 mL of tetrahydrofuran, precipitated into 800 mL of hexanes, filtered, washed well with hexanes, and dried in a vacuum oven at 40° C. for 24 hours. Yield 19.8 g (79% of theory). Composition of the title terpolymer was determined by quantitative C-13 NMR and was found to be within experimental error of the monomer feed ratio.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07090968B2uspto-grants-2006_08