Reaktion #1458432

ord-20ed51f39d5d486786a0506c36e8ee28

Reaktionsgleichung

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

Reagenzien

Keine

Reaktionsbedingungen

Temperatur
30°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISSOLUTIONdissolved at 50° C
  2. 2
    FiltrationThe mixture was filtrated through a 10 μm
  3. 3
    Filtrationfilter
  4. 4
    Sonstigerecrystallization
  5. 5
    TemperaturCooling speed
  6. 6
    Sonstigefor the recrystallization
  7. 7
    FiltrationThe resulting crystal was subjected to centrifugal filtration
  8. 8
    Waschenwashing
  9. 9
    Sonstigethe aforementioned recrystallization procedure twice additionally
  10. 10
    SonstigeThereafter, the crystal was dried
  11. 11
    SonstigeThus resulting crystal
  12. 12
    Sonstigeto give the

Vorschrift

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 %.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07157217B2uspto-grants-2007_01