Reacción #1375808

ord-7e740a55812f4c5ea46d2cbd9fad1134

Ecuación de reacción

CC(=O)OCc1c2ccccc2c(COC(C)=O)c2ccccc12
acetic
CC(=O)OCc1c2ccccc2c(COC(C)=O)c2ccccc12
acetic
C=CC=O
acrolein

Reactantes

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONadd
  2. 2
    workup.DISTILLATIONdistillation column
  3. 3
    workup.DISTILLATIONa distillation column
  4. 4
    workup.DISTILLATIONfor effectively reducing, by its distillation, acetic acid from the CAA
  5. 5
    workup.DISTILLATIONDistillation of the Group
  6. 6
    workup.ADDITIONA-treated CAA

Procedimiento

Another embodiment of the invention utilizing the same amine groups in similar manner is the addition of one or more amine of Group A to a CAA having a high (>2,000 ppm) level of acetic acid. This high acetic acid-containing CAA feed stream may be fed to an acetic add distillation column, that is, a distillation column used for effectively reducing, by its distillation, acetic acid from the CAA. Distillation of the Group A-treated CAA yields a low acrolein (also now low acetic add) CAA. (The Group A amine can be fed to the acetic acid removal column as a separate stream as the high acetic acid CAA is fed to the column.) Subsequently, the low acrolein CAA is fed to a final distillation column, i.e., a high purity acrylic acid distillation column, where the final distillation steps, previously described, are carried out.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05746892uspto-grants-1998_05