Reacción #2356

ord-2f67cb89cb8f4479a6231aded45cb5b0

Disolventes

Condiciones de reacción

Temperatura
140°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA flame dried
  2. 2
    OtroThe flask was fitted with a flame
  3. 3
    Otrodried mechanical stirrer
  4. 4
    OtroThe flask was purged with nitrogen three times
  5. 5
    Temperaturamaintained at this temperature for about 24 hours
  6. 6
    TemperaturaThe reaction mixture was then cooled to 110° C.
  7. 7
    Temperaturamaintained at this temperature for 24 hours
  8. 8
    OtroThe copolymer was dried under vacuum (0.1 mm Hg) at 80° C. for about 32 hours
  9. 9
    Otroto remove any unreacted monomer
  10. 10
    Otroat 250° C
  11. 11
    Otroat room temperature

Procedimiento

A flame dried, 250 mL, round bottom single neck flask was charged with 57.1 grams (0.50 mole) of ε-caprolactone, 51.0 grams (0.50 mole) of p-dioxanone, 4.00 mL (55 mmol) of distilled glycerol, and 0.12 mL (40 μmol) of a 0.33M stannous octoate solution in toluene. The flask was fitted with a flame dried mechanical stirrer. The flask was purged with nitrogen three times before venting with nitrogen. The reaction mixture was heated to 140° C. and maintained at this temperature for about 24 hours. The reaction mixture was then cooled to 110° C. and maintained at this temperature for 24 hours. The copolymer was dried under vacuum (0.1 mm Hg) at 80° C. for about 32 hours to remove any unreacted monomer. The copolymer had an inherent viscosity of 0.14 dL/g in HFIP at 250° C. The copolymer was a liquid at room temperature. The molar ratio of PCL/PDS was found to be 53.2/46.8 by proton NMR.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05728752uspto-grants-1998_03