Reaction #1904043

ord-d21b99ba0051478fab22b87c296849b2

Reaction equation

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
Yield 72.4%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureIt was heated at 200 degrees Centigrade
  2. 2
    Temperaturerefluxed for 12 hours until no peaks of starting materials and intermediates
  3. 3
    workup.ADDITIONto disperse
  4. 4
    FiltrationIt was filtrated
  5. 5
    Washwashed with water
  6. 6
    OtherPrecipitated crystals
  7. 7
    Otherwere purified by silica gel column chromatography

Procedure

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07598010B2uspto-grants-2009_10