Reacción #1256723

ord-3d322a73b98d45699bdee5ef9869b9d5

Ecuación de reacción

CCCC1CCC(=O)C(C(=O)OC)C1
methyl 2-oxo-5-propylcyclohexanecarboxylate
Oc1cccc(O)c1
resorcinol
O=P(Cl)(Cl)Cl
phosphoryl chloride
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCI
ethyl iodide
CCCC1CCc2c(c(=O)oc3cc(OCC)ccc23)C1
3-ethoxy-8-propyl-7,8,9,10-tetrahydrobenzo[c]chromen-6-one

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture is heated
  2. 2
    Temperaturaunder reflux for 3 h
  3. 3
    OtroAfter hydrolysis
  4. 4
    Filtraciónthe deposited precipitate is filtered off with suction
  5. 5
    Lavadowashed with toluene
  6. 6
    Otrodried
  7. 7
    workup.DISSOLUTIONThe product is dissolved in 200 ml of acetone
  8. 8
    Temperaturathe mixture is heated
  9. 9
    Temperaturaunder reflux for 5 h
  10. 10
    OtroThe majority of the solvent is removed under reduced pressure
  11. 11
    OtroThe aqueous phase is separated off
  12. 12
    Extracciónextracted with MTB ether
  13. 13
    LavadoThe combined organic phases are washed with water
  14. 14
    Secadodried over sodium sulfate
  15. 15
    OtroThe solvent is removed under reduced pressure
  16. 16
    Otrothe crude product is recrystallised from ethanol

Procedimiento

16.6 g (78.5 mmol) of methyl 2-oxo-5-propylcyclohexanecarboxylate, 7.65 g (69.5 mmol) of resorcinol and 5.6 ml (6.1 mmol) of phosphoryl chloride are dissolved in 55 ml of toluene, and the mixture is heated under reflux for 3 h. After hydrolysis using water, the deposited precipitate is filtered off with suction, washed with toluene and dried. The product is dissolved in 200 ml of acetone, 20 g (145 mmol) of potassium carbonate and 9.00 g (57.7 mmol) of ethyl iodide are added, and the mixture is heated under reflux for 5 h. The majority of the solvent is removed under reduced pressure, and the residue is taken up in MTB ether/water. The aqueous phase is separated off and extracted with MTB ether. The combined organic phases are washed with water and dried over sodium sulfate. The solvent is removed under reduced pressure, and the crude product is recrystallised from ethanol, giving 3-ethoxy-8-propyl-7,8,9,10-tetrahydrobenzo[c]chromen-6-one as colourless crystals. The melting point is 108° C. The other physical properties are: Δ∈=−7.5 (extrapolated from 5% solution in ZLI-2857), Δn=0.1302 (5% in ZLI-4792).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07824745B2uspto-grants-2010_11