Reacción #84865
ord-e3e0bb67c1f143f98cc36cc349d6eddc
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ExtracciónIt was then extracted with EtOAc twice
- 2Lavadothe combined organics were washed with H2O and brine
- 3Secadodried over Na2SO4
- 4Concentraciónconcentrated
- 5OtroPurification by chromatography (30% EtOAc-hexanes)
Procedimiento
A solution of 2-bromo-1-(4-bromo-3,5-dimethoxyphenyl)propan-1-one (1.07 g, 3.04 mmol) in formamide (10 mL) in an oven-dried flask under argon was heated at 110° C. for 16 hrs. After cooling to room temp, EtOAc and saturated aqueous NaHCO3 were carefully added and the mixture was stirred for 15 minutes. It was then extracted with EtOAc twice and the combined organics were washed with H2O and brine, dried over Na2SO4 and concentrated. Purification by chromatography (30% EtOAc-hexanes) gave 4-(4-bromo-3,5-dimethoxyphenyl)-5-methyloxazole as a yellow solid (0.496 g, 55% yield).