Reacción #1797507

ord-68c035e209c4465593320516e387ba1c

Ecuación de reacción

O
Water
Oc1cccc(Br)c1
3-Bromophenol
O=[N+]([O-])[O-].[Na+]
sodium nitrate
O
water
O=[N+]([O-])c1ccc(Br)cc1O
title compound
Rendimiento 20.0%
O=[N+]([O-])c1ccc(Br)cc1O
5-bromo-2-nitrophenol
Rendimiento 20.0%

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthe resulting mixture was extracted with diethyl ether
  2. 2
    Secadothe extract was dried (MgSO4)
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated
  5. 5
    OtroThe residue was purified by flash chromatography (silica gel, 10% ethyl acetate/hexanes)

Procedimiento

3-Bromophenol (32.9 g, 0.19 mol) was added slowly to a cold (10° C.) solution of sodium nitrate (29.0 g, 0.34 mol) in conc. sulfuric acid; (40.0 g) and water (70.0 mL) and the resulting mixture was allowed to stir at room temperature for 2 h. Water (200 mL) was added and the resulting mixture was extracted with diethyl ether and the extract was dried (MgSO4), filtered and concentrated. The residue was purified by flash chromatography (silica gel, 10% ethyl acetate/hexanes) to afford first the title compound (8.1 g, 20%), mp 40-42° C., then the undesired isomer, 3-bromo-4-nitrophenol, as a yellow solid (12.7 g, 31%). mp 125-127° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07790704B2uspto-grants-2010_09