Reacción #54964
ord-15c03e503fec4509a2e2f164f7947f2d
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Otrofor a total of 48 hours
- 2OtroThe catalyst was removed by filtration (`Hyflo` supercel) and the ethanol
- 3Otroremoved in vacuo
- 4Otroaffording an oil
- 5OtroThe excess oxidant was destroyed with methanol
- 6workup.DISSOLUTIONthe reaction mixture was dissolved in water (200 ml)
- 7Extracciónextracted with ether
- 8LavadoThe combined ethereal extracts were washed with water, dilute aqueous sodium bicarbonate solution and water
- 9Secadodried (MgSO4)
- 10Concentraciónconcentrated 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.