Reacción #7804

ord-10019520ef6f48319b08b25838da63f4

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction was refluxed for 30 min
  2. 2
    Otrothe excess of SOCl2 was removed in vacuo
  3. 3
    workup.DISSOLUTIONThe oily acid chloride was dissolved in THF (15 mL)
  4. 4
    TemperaturaThe reaction was then warmed to rt for 1 h
  5. 5
    Otrothe precipitate was removed by filtration
  6. 6
    ConcentraciónThe filtrate was concentrated
  7. 7
    Otrodried in vacuo
  8. 8
    workup.DISSOLUTIONthe dark brown solid residue was dissolved in toluene (20 mL)
  9. 9
    TemperaturaThe reaction was refluxed overnight
  10. 10
    Temperaturacooled to rt
  11. 11
    LavadoThe organic solution was washed with brine (3×50 mL)
  12. 12
    Secadodried (MgSO4)
  13. 13
    Filtraciónfiltered
  14. 14
    Concentraciónconcentrated in vacuo
  15. 15
    OtroThe residue was recrystallized in EtOAc

Procedimiento

To a 100 mL round-bottom flask with 3-hydroxy-4-methylbenzoic acid (2.5 g, 16.4 mmol), was added SOCl2 (15 mL) dropwise. The reaction was refluxed for 30 min, cooled to rt and the excess of SOCl2 was removed in vacuo. The oily acid chloride was dissolved in THF (15 mL) and the solution was added dropwise to a mixture of 2-aminophenol (1.8 g, 16.4 mmol), triethylamine (1.7 g, 16.4 mmol) and THF (30 mL) at 0° C. The reaction was then warmed to rt for 1 h and the precipitate was removed by filtration. The filtrate was concentrated and dried in vacuo and the dark brown solid residue was dissolved in toluene (20 mL) and p-toluenesulfonic acid (15.6 g, 82 mmol) was added. The reaction was refluxed overnight, cooled to rt and dissolved in EtOAc (500 mL). The organic solution was washed with brine (3×50 mL), dried (MgSO4), filtered, and concentrated in vacuo. The residue was recrystallized in EtOAc to afford 5-(1,3-benzoxazol-2-yl)-2-methylphenol as a light yellow solid. MS (ESI) 226 (M+H)+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07087601B2uspto-grants-2006_08