Reacción #89918

ord-d8b566cb3796403ca89b43a01101efa7

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITat RT for 3 hours
  2. 2
    ExtracciónThe mixture was extracted with CH2Cl2 (3×200 mL)
  3. 3
    SecadoThe combined organics were dried (Na2SO4)
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated in vacuo
  6. 6
    OtroThe residue was azeotroped with heptane

Procedimiento

To a solution of benzyl 3-(benzyloxy)-4-methoxybenzoate (6.32 g, 18.1 mmol) in Ac2O (62 mL) cooled to −10° C. under an atmosphere of N2 was added fuming HNO3 (1.5 mL, 37.1 mmol) in one portion. Stirring was continued at −10° C. for 10 minutes, then at RT for 3 hours. The reaction mixture was carefully poured into ice-water and the pH adjusted to ca. pH=5 with 5N NaOH, sat. NaHCO3 and 0.5 NaOH. The mixture was extracted with CH2Cl2 (3×200 mL). The combined organics were dried (Na2SO4), filtered and concentrated in vacuo. The residue was azeotroped with heptane to give benzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate as red colored oil (6.55 g, 16.7 mmol, 93%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09440961B2uspto-grants-2016_09