Reacción #1904043

ord-d21b99ba0051478fab22b87c296849b2

Ecuación de reacción

Ic1ccc(-c2ccc(I)cc2)cc1
4,4′-diiodobiphenyl
O=C([O-])[O-].[K+].[K+]
potassium carbonate
c1ccc(Nc2ccc3ccccc3c2)cc1
N-phenyl-2-naphthylamine
CN(C)C=O
DMF
c1ccc(N(c2ccc(-c3ccc(N(c4ccccc4)c4ccc5ccccc5c4)cc3)cc2)c2ccc3ccccc3c2)cc1
beta-NPD
Rendimiento 72.4%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaIt was heated at 200 degrees Centigrade
  2. 2
    Temperaturarefluxed for 12 hours until no peaks of starting materials and intermediates
  3. 3
    workup.ADDITIONto disperse
  4. 4
    FiltraciónIt was filtrated
  5. 5
    Lavadowashed with water
  6. 6
    OtroPrecipitated crystals
  7. 7
    Otrowere purified by silica gel column chromatography

Procedimiento

25.1 g (61.5 mmol) of 4,4′-diiodobiphenyl, 2.14 g of poly(ethylene glycol) PEG-6000 that was available from Wako Pure Chemical Industries, Ltd., 17.1 g (0.124 mol) of potassium carbonate and 15.7 g (247 mmol) of powdered copper were added to 32.4 g (148 mmol) of N-phenyl-2-naphthylamine. It was heated at 200 degrees Centigrade. It was determined for tracing by the high-speed liquid chromatography. And it was stirred and refluxed for 12 hours until no peaks of starting materials and intermediates were determined. DMF and water were added thereto to disperse. It was filtrated and washed with water. Precipitated crystals were purified by silica gel column chromatography to obtain 26.2 g of beta-NPD that is represented by Compound Example 5 at 72.4% yield.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07598010B2uspto-grants-2009_10