Reacción #2439929
ord-a0d41e915711416f8c03b6f1830fb910
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Otroevaporating the solvent to dryness
- 2workup.DISSOLUTIONThe hot clear viscous residue was dissolved in an equal volume of dichloromethane
- 3Otroprecipitated in a mixture of ether/petroleum ether (1:1 v/v)
- 4FiltraciónThe white precipitate was collected by filtration
- 5Otrodried by vacuum at room temperature
- 6OtroAcetyl terminated fatty acid anhydrides
- 7Otrowere prepared
- 8Temperaturarefluxing for 20 min
- 9Otrowere prepared
- 10Otroevaporating the solvent to dryness
- 11Otroto 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.