Reacción #1519097

ord-f6cb9cc586a342d7993bb5fdd588c875

Ecuación de reacción

CO
methanol
[H-].[Na+]
sodium hydride
O=C1Nc2ccccc2C1=O
Isatin
O=C1C(=O)N(c2ccc(C3OC=CO3)cc2)c2ccccc21
N-[4-(1,3-dioxolyl)phenyl]isatin

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThis suspension was heated in an oil-bath at 135° C. under nitrogen for 16 hours
  2. 2
    TemperaturaIt was then cooled to room temperature
  3. 3
    FiltraciónThe resulting suspension was filtered
  4. 4
    Concentraciónthe filtrate was concentrated under reduced pressure
  5. 5
    Otroevaporated to dryness
  6. 6
    OtroA thick, viscous oil was recovered which
  7. 7
    Otrosuch for the next reaction

Procedimiento

Isatin (1.88 g, 0.0128 moles) in anhydrous DMF (100 mL) was cooled in an ice bath under nitrogen and treated with sodium hydride (0.3 g, 1 equivalent). The reaction was warmed to room temperature and stirred for 1 hour. It was then treated with 2-(4-bromophenyl)-1,3-dioxalane (2.83 g, 0.0124 moles) followed by CuI (4.71 g, 2 equivalents). This suspension was heated in an oil-bath at 135° C. under nitrogen for 16 hours. It was then cooled to room temperature and diluted with an equal volume of chloroform. The resulting suspension was filtered and the filtrate was concentrated under reduced pressure. The residue was suspended in xylenes (100 mL) and evaporated to dryness. A thick, viscous oil was recovered which was used as such for the next reaction. TLC (5% methanol in chloroform) showed clean conversion, Rf (product)=0.91.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07611909B1uspto-grants-2009_11