Reaktion #4075

ord-e48263ea1c184915ac82de02fc1d25d1

Reaktionsgleichung

CCOC(=O)CC(C)=O
ethyl acetoacetate
CC(=O)C=C(C)C
mesityl oxide
CCCCCCC
heptane
CCOC(=O)C1C(C)=CC(=O)CC1(C)C
ester
Ausbeute 27.0%
CCOC(=O)C1C(C)=CC(=O)CC1(C)C
Ethyl 4-Oxo-2,6,6-Trimethylcyclohex-2-Ene-1-Carboxylate
Ausbeute 27.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturat reflux in a 5000 ml round bottom flask
  3. 3
    SonstigeThe flask was equipped with a Dean-Stark trap
  4. 4
    Sonstigedrying tube
  5. 5
    workup.ADDITIONan additional 25 g of zinc chloride was added
  6. 6
    Temperaturrefluxing
  7. 7
    workup.WAITcontinued for 36 h
  8. 8
    TemperaturAfter cooling
  9. 9
    Waschenthe reaction mixture was washed with 1500 ml of water, 5% sodium bicarbonate solution (2×1000 ml)
  10. 10
    SonstigeRemoval of solvent
  11. 11
    Sonstigeby evaporation
  12. 12
    Sonstigeyielded 979 g of crude product
  13. 13
    workup.DISTILLATIONDistillation of the crude product

Vorschrift

A mixture of 1020 ml (1041 g, 8.00 mol) of ethyl acetoacetate, 960 ml (824 g, 8.40 mol) of mesityl oxide, 1000 ml of heptane, 600 ml of toluene, and 175 g of zinc chloride was heated at reflux in a 5000 ml round bottom flask while stirring. The flask was equipped with a Dean-Stark trap and drying tube. After 24 h, an additional 25 g of zinc chloride was added and refluxing continued for 36 h. After cooling, the reaction mixture was washed with 1500 ml of water, 5% sodium bicarbonate solution (2×1000 ml), and another 1500 ml of water. Removal of solvent by evaporation yielded 979 g of crude product. Distillation of the crude product provided 453.5 g of the desired ester which represents 27.0% yield. Distillation was at 124°-5° C. (3.0 torr).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04723038uspto-grants-1988_02