Aromatic amine derivative and application thereof
An aromatic amine and derivative technology, applied in electrical components, circuits, organic chemistry, etc., can solve the problems of short life and high voltage, and achieve the effects of reducing crystallinity, reducing planarity, and improving exciton utilization.
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[0050] Preparation of reactant A-1
[0051]
[0052] In a 250ml three-neck flask, under the protection of nitrogen, add 0.01mol raw material X-1, 0.01mol raw material X-2, 150ml toluene and stir to mix, then add 5×10 -5 mol Pd 2 (dba) 3 , 5×10 -5 mol P(t-Bu) 3 , 0.03mol sodium tert-butoxide, heated to 105°C, refluxed for 12 hours, sampled on the plate, showed no bromide remaining, and the reaction was complete; naturally cooled to room temperature, filtered, the filtrate was rotary evaporated to no fraction, passed through a neutral silica gel column , to obtain reactant A-1, HPLC purity 99.31%, yield 79.55%;
[0053] Elemental analysis structure (C 20 h 15 N) Theoretical: C, 89.19; H, 5.61; N, 5.20; Tested: C, 89.20; H, 5.59; N, 5.21. LC-MS: The theoretical value is 269.12, and the measured value is 269.41.
[0054] The preparation method of other reactant A is similar to the preparation method of reactant A-1, the difference lies in the difference of raw materials...
Embodiment 1
[0055] The preparation of embodiment 1 compound 33
[0056]
[0057] (1) In a 250ml three-neck flask, under the protection of nitrogen, add 0.01mol reactant A-1, 0.01mol reactant B-1, 150ml toluene and stir to mix, then add 5×10 -5 mol Pd 2 (dba) 3 , 5×10 -5 mol P(t-Bu) 3 , 0.03mol sodium tert-butoxide, heated to 110°C, refluxed for 16 hours, sampled on the plate, showed no bromide remaining, and the reaction was complete; naturally cooled to room temperature, filtered, the filtrate was rotary evaporated to no fraction, passed through a neutral silica gel column , to obtain intermediate C-1;
[0058] (2) In a 250ml three-neck flask, under the protection of nitrogen, add 0.01mol intermediate C-1, 0.01mol reactant A-2, 150ml toluene and stir to mix, then add 5×10 -5 mol Pd 2 (dba) 3 , 5×10 -5 mol P(t-Bu) 3 , 0.03mol sodium tert-butoxide, heated to 120°C, refluxed for 20 hours, sampling plate, showed no bromide remaining, the reaction was complete; naturally cooled to...
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