Reacción #1458432

ord-20ed51f39d5d486786a0506c36e8ee28

Ecuación de reacción

CC(C)O
isopropyl alcohol
CCCCCCCCCCCCCCCCCCCCCC(=O)O
Behenic acid
CCCCCCCCCCCCCCCCCCCC(=O)O
arachidic acid
CCCCCCCCCCCCCCCCCCCCCCCC(=O)O
lignoceric acid
CCCCCCCCCCCCCCCCCCCCCC(=O)O
behenic acid

Reactivos

Ninguno

Condiciones de reacción

Temperatura
30°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISSOLUTIONdissolved at 50° C
  2. 2
    FiltraciónThe mixture was filtrated through a 10 μm
  3. 3
    Filtraciónfilter
  4. 4
    Otrorecrystallization
  5. 5
    TemperaturaCooling speed
  6. 6
    Otrofor the recrystallization
  7. 7
    FiltraciónThe resulting crystal was subjected to centrifugal filtration
  8. 8
    Lavadowashing
  9. 9
    Otrothe aforementioned recrystallization procedure twice additionally
  10. 10
    OtroThereafter, the crystal was dried
  11. 11
    OtroThus resulting crystal
  12. 12
    Otroto give the

Procedimiento

Behenic acid manufactured by Henkel Co. (trade name: Edenor C22-85R) in an amount of 100 kg was admixed with 1200 kg of isopropyl alcohol, and dissolved at 50° C. The mixture was filtrated through a 10 μm filter, and cooled to 30° C. to allow recrystallization. Cooling speed for the recrystallization was controlled to be 3° C./hour. The resulting crystal was subjected to centrifugal filtration, and washing was performed with 100 kg of isopropyl alcohol, followed by repeating the aforementioned recrystallization procedure twice additionally. Thereafter, the crystal was dried. Thus resulting crystal was esterified, and subjected to GC-FID analysis to give the results of the content of behenic acid being 96 mol %, lignoceric acid 2 mol % and arachidic acid 2 mol %. In addition, erucic acid was included at 0.001 mol %.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07157217B2uspto-grants-2007_01