Novel compound and organic electroluminescent device comprising the same
A technology of organic light-emitting elements and compounds, which is applied in the field of new compounds, can solve the problems of not easy to be practical, high driving voltage, short service life, etc., and achieve excellent long-life characteristics, low voltage, and prevent the increase of conjugated length Effect
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manufacture example 1
[0106] Synthesis of Compound 10
[0107]
[0108] Under an argon or nitrogen atmosphere, 10 g of reactant (1), 12 g of reactant (2), 0.9 g of Tetrakis (triphenyl phosphine) palladium (0) were mixed with a 250 ml volumetric flask. )) was dissolved in 50 ml of dioxane, followed by adding a solution in which 11.2 g of sodium carbonate was dissolved in 20 ml of water, followed by heating and stirring for 24 hours.
[0109] After the reaction was completed, it was cooled to room temperature and the precipitated crystals were separated by filtration. It was recrystallized from toluene to synthesize 6.5 g (40%) of compound 10.
[0110] 1H-NMR (CDCl3, 400MHz): δ1.71(6H,s), 6.43(2H,d), 6.90-7.00(4H,m), 6.90-7.68(17H,m), 7.69(1H,d), 7.89(1H,s), 8.00(1H,s), 8.15(2H,d)
[0111] LC-MS Purityis 99.91%, Rt=2.67 min; MS Calcd.: 602.76; MS Found: 602 [M].
manufacture example 2
[0112] Synthesis of Compound 60
[0113]
[0114] Compound 60 was synthesized by the same method as in Production Example 1 using the reactant (3) in place of the reactant (2).
[0115] MS Calcd.: 603.27; MS Found: 603.4 [M].
manufacture example 3
[0116] Synthesis of Compound 1
[0117]
[0118] Compound 1 was synthesized by the same method as in Production Example 1 using the reactant (4) in place of the reactant (1) and the reactant (5) in place of the reactant (2).
[0119] MS Calcd.: 602.76; MS Found: 602 [M].
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