Compound taking anthrone skeleton as core, and application thereof
A technology of compounds and skeletons, applied in organic chemistry, chemical instruments and methods, electrical components, etc., can solve problems such as performance differences, and achieve the effects of improving the use of processing windows, improving current efficiency and life, and strong rigidity
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[0068] Preparation of reactant B-1
[0069]
[0070] (1) In a 250mL three-necked flask, under the protection of nitrogen, add 0.01mol of raw material X-1, 0.012mol of raw material X-2, 150mL of toluene, and stir and mix, then add 0.03mol of sodium tert-butoxide, 5 × 10 -5 molPd 2 (dba) 3 , 5×10 -5 mol tri-tert-butylphosphine, heated to 105 ° C, refluxed for 24 hours, the reaction was complete; naturally cooled to room temperature, filtered, the filtrate was subjected to vacuum rotary evaporation (-0.09MPa, 85 ° C), and passed through a neutral silica gel column to obtain an intermediate body Y-1;
[0071] (2) 250mL three-necked flask, under the atmosphere of feeding nitrogen, add 0.02mol intermediate Y-1, 40mL tetrahydrofuran to dissolve completely, cool to -78 ℃, then add 15mL of 1.6mol / L n-butane to the reaction system The tetrahydrofuran solution of base lithium was reacted at -78 °C for 3 hours, and then 0.024 mol of triisopropyl borate was added, and the reaction w...
Example Embodiment
[0080] Preparation of Example 1 Compound 2
[0081]
[0082] 250mL three-necked flask, under the atmosphere of feeding nitrogen, add 0.01mol reactant A-1, 0.015mol reactant B-1, dissolve with mixed solvent (90mL toluene, 45mL ethanol), then add 0.03mol Na 2 CO 3 Aqueous solution (2M), stirred with nitrogen for 1 hour, then added 0.0001mol Pd (PPh 3 ) 4 , heated to reflux for 15 hours, sampling point plate, the reaction was complete. Naturally cooled, filtered, the filtrate was rotary evaporated, and passed through a silica gel column to obtain compound 2; the yield was 76.06%, and the HPLC purity was 98.72%.
[0083] Elemental analysis structure (molecular formula C 61 H 37 N 3 O 2 ): Theoretical: C, 86.81; H, 4.42; N, 4.98; Tested: C, 86.82; H, 4.40; N, 4.99. LC-MS: Theoretical value is 843.29, and the found value is 843.22.
[0084] The preparation procedure of Example 1 was repeated to synthesize the following compounds, except that reactants A and B listed in T...
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