Reacción #54964

ord-15c03e503fec4509a2e2f164f7947f2d

Ecuación de reacción

CCc1oc2ccc(C(C)C(=O)OC)cc2c(=O)c1C
Methyl 2-[2-ethyl-3-methyl-4-oxo-4H-1-benzopyran-6-yl]propionate
CC(C)=O.O=S(=O)(O)O.[O]=[Cr](=[O])=[O]
Jones reagent
O=S(=O)([O-])[O-].[Ba+2]
barium sulphate
CCC1Oc2ccc(C(C)C(=O)OC)cc2C(=O)C1C
title compound
CCC1Oc2ccc(C(C)C(=O)OC)cc2C(=O)C1C
Methyl 2-[2,3-dihydro-2-ethyl-3-methyl-4-oxo-4H-1-benzopyran-6-yl]propionate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrofor a total of 48 hours
  2. 2
    OtroThe catalyst was removed by filtration (`Hyflo` supercel) and the ethanol
  3. 3
    Otroremoved in vacuo
  4. 4
    Otroaffording an oil
  5. 5
    OtroThe excess oxidant was destroyed with methanol
  6. 6
    workup.DISSOLUTIONthe reaction mixture was dissolved in water (200 ml)
  7. 7
    Extracciónextracted with ether
  8. 8
    LavadoThe combined ethereal extracts were washed with water, dilute aqueous sodium bicarbonate solution and water
  9. 9
    Secadodried (MgSO4)
  10. 10
    Concentraciónconcentrated in vacuo

Procedimiento

Methyl 2-[2-ethyl-3-methyl-4-oxo-4H-1-benzopyran-6-yl]propionate (6.61 g) was taken up in dry ethanol (150 ml) and hydrogenated at 85 p.s.i. with 5% palladium on carbon (0.2 g) and 5% palladium on barium sulphate (0.49) for a total of 48 hours. The catalyst was removed by filtration (`Hyflo` supercel) and the ethanol removed in vacuo affording an oil. The oil was taken up in acetone (50 ml) and treated with a slight excess of Jones reagent. The excess oxidant was destroyed with methanol and the reaction mixture was dissolved in water (200 ml) and extracted with ether. The combined ethereal extracts were washed with water, dilute aqueous sodium bicarbonate solution and water, dried (MgSO4) and concentrated in vacuo to give the title compound as an oil--6 g.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04151179uspto-grants-1979_04