Reacción #2439929

ord-a0d41e915711416f8c03b6f1830fb910

Ecuación de reacción

CCCCCCCC/C=C\CCCCCCCC(=O)O
oleic acid
CCCCC/C=C\C/C=C\CCCCCCCC(=O)O
linoleic acid
CC(=O)OC(C)=O
acetic anhydride
CC(=O)OC(C)=O
acetic anhydride
CC(=O)OC(C)=O
acetic anhydride
O=C(O)CCCCCCCCC(=O)O
sebacic acid

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroevaporating the solvent to dryness
  2. 2
    workup.DISSOLUTIONThe hot clear viscous residue was dissolved in an equal volume of dichloromethane
  3. 3
    Otroprecipitated in a mixture of ether/petroleum ether (1:1 v/v)
  4. 4
    FiltraciónThe white precipitate was collected by filtration
  5. 5
    Otrodried by vacuum at room temperature
  6. 6
    OtroAcetyl terminated fatty acid anhydrides
  7. 7
    Otrowere prepared
  8. 8
    Temperaturarefluxing for 20 min
  9. 9
    Otrowere prepared
  10. 10
    Otroevaporating the solvent to dryness
  11. 11
    Otroto obtain a liquid

Procedimiento

The prepolymer of sebacic acid (SA) was prepared from the purified diacid monomer by refluxing in excess acetic anhydride for 30 minutes and evaporating the solvent to dryness. The hot clear viscous residue was dissolved in an equal volume of dichloromethane and precipitated in a mixture of ether/petroleum ether (1:1 v/v). The white precipitate was collected by filtration and dried by vacuum at room temperature. Acetyl terminated fatty acid anhydrides were prepared by dissolving the acids in acetic anhydride (120° C., 1:5 w/v) and refluxing for 20 min. Acetate anhydrides of oleic acid, linoleic acid and other cis-double bond containing fatty acid were prepared by refluxing the fatty acid in acetic anhydride for 20 min. and evaporating the solvent to dryness to obtain a liquid. Mixed prepolymers of diacids with the monoacid terminals were prepared similarly.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07749539B2uspto-grants-2010_07