Reaktion #347316

ord-dfd6bab83436493486bd1a795b68e9ad

Reaktionsgleichung

CCCCCCCCCCCCCCCC(=O)O
Palmitic acid
CC(=O)OC(C)=O
acetic anhydride
CCCCCCCCCCCCCCCC(=O)O
palmitic acid
CCCCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCCCC
Palmitic Anhydride

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigefitted with an overhead stirrer
  2. 2
    TemperaturThe mixture was heated gently
  3. 3
    Sonstige(61° C. to 64° C.)
  4. 4
    TemperaturHeating
  5. 5
    Sonstige(147° C.)
  6. 6
    Temperaturthis temperature was maintained for a period of one hour
  7. 7
    Sonstigeto form
  8. 8
    Filtrationfiltered
  9. 9
    Sonstigerecrystallised from petroleum ether 60-80
  10. 10
    Sonstigewas placed in a vacuum oven at 40° C.
  11. 11
    Trocknenuntil dry of residual acetic acid

Vorschrift

Palmitic acid (512.04 g, 2.00 moles) and acetic anhydride (204.05 g, 2.00 moles) were charged to a two liter reaction flask fitted with an overhead stirrer, thermometer, condenser and nitrogen inlet. The mixture was heated gently with stirring to allow the solid palmitic acid to melt (61° C. to 64° C.). Heating was continued until the reflux temperature had been reached (147° C.), this temperature was maintained for a period of one hour. The resultant mixture was cooled to room temperature to allow a light yellow solid to form, this was slurried in cyclohexane (100 ml), filtered and recrystallised from petroleum ether 60-80. The recrystallised wet solid was placed in a vacuum oven at 40° C. until dry of residual acetic acid. The resultant white powdery solid was stored under vacuum in the presence of silica gel. The yield of palmitic anhydride was 458.49 g which represented a 92.8% chemical yield.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05525709uspto-grants-1996_06