Reacción #487493

ord-7c9cefd0e4c943f7a4d77c843d4d4589

Ecuación de reacción

COC(=O)c1ccc(C(=O)OC)cc1
Dimethyl terephthalate
CCCCCCCCCCCCCCCCCCO
Stearyl Alcohol
CCCCCCCCCCCCCCCCCCOC(=O)c1ccc(C(=O)OCCCCCCCCCCCCCCCCCC)cc1
white solid
Rendimiento 96.2%
CCCCCCCCCCCCCCCCCCOC(=O)c1ccc(C(=O)OCCCCCCCCCCCCCCCCCC)cc1
distearyl terephthalate
Rendimiento 96.2%

Reactivos

Ninguno

Condiciones de reacción

Temperatura
130°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroTo a 2 L Buchi reactor equipped with a double turbine agitator and distillation apparatus
  2. 2
    Otropurge for 1 hour
  3. 3
    workup.ADDITIONwas commenced followed by the addition of Tyzor catalyst (3.0 grams, available from Dupont)
  4. 4
    TemperaturaThe reaction mixture was then heated to 145° C.
  5. 5
    Otroto 190° C.
  6. 6
    Otroover a 3-4 hour
  7. 7
    workup.DISTILLATIONis distilled in a controlled manner
  8. 8
    TemperaturaThe reaction temperature was maintained at 190° C. for an additional 16 hours until >96% conversion to the product
  9. 9
    Temperaturaon cooling

Procedimiento

To a 2 L Buchi reactor equipped with a double turbine agitator and distillation apparatus was charged Dimethyl terephthalate (315.8 grams), Stearyl Alcohol (879.7 grams) and heated to 130° C. under Nitrogen purge for 1 hour, after which stirring was commenced followed by the addition of Tyzor catalyst (3.0 grams, available from Dupont). The reaction mixture was then heated to 145° C., followed by slowly ramping the temperature to 190° C. over a 3-4 hour period such that the evolution of methanol is distilled in a controlled manner. The reaction temperature was maintained at 190° C. for an additional 16 hours until >96% conversion to the product was achieved as determined by 1H NMR spectroscopy. The product was discharged as a low viscosity liquid which solidified on cooling to give a 1050 gram of a white solid (96.2% yield). The product was shown to be pure by 1H NMR spectroscopy with trace amounts of the mono-ester. Physical properties of this compound are shown in Table 2.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08741043B2uspto-grants-2014_06