Organic compound containing benzanthracene, preparation method and application thereof
An organic compound and benzanthracene technology, applied in the field of benzanthracene-containing organic compounds and their preparation, can solve problems such as differences, achieve high glass transition temperature, structure optimization, and meet application requirements.
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preparation example Construction
[0067] The preparation of raw material A refers to the preparation method of the above raw material A1, and the synthetic raw materials of raw material A required in the examples are shown in Table 1:
[0068] Table 1
[0069]
[0070]
Embodiment 1
[0071] Embodiment 1: the synthesis of compound 1:
[0072]
[0073] In a 250ml three-neck flask, under the protection of nitrogen, add 0.01mol raw material A1, 0.012mol reactant B1, 150ml toluene and stir to mix, then add 5×10-5mol Pd2(dba)3, 5×10-5mol P(t- Bu)3, 0.03mol sodium tert-butoxide, heated to 105°C, refluxed for 24 hours, sampling plate, showed no bromide remaining, the reaction was complete; naturally cooled to room temperature, filtered, the filtrate was rotary evaporated to no fraction, and passed The target product was obtained on a permanent silica gel column with a HPLC purity of 99.76% and a yield of 76.1%. Elemental analysis structure (molecular formula C 46 h 27 N): theoretical value: C, 93.06; H, 4.58; N, 2.36; test value C, 93.04; H, 4.57; N, 2.39. MS (m / z) (M+): theoretical value 593.21, found value 593.44.
Embodiment 2
[0074] Embodiment 2: the synthesis of compound 5:
[0075]
[0076] Prepare by the synthetic method of compound 1 in embodiment 1, difference is to replace reactant B1 with reactant B2; Elemental analysis structure (molecular formula C 48 h 27 NO): Theoretical: C, 90.97; H, 4.29; N, 2.21; O, 2.52; Tested: C, 90.95; H, 4.28; N, 2.26. MS (m / z) (M+): theoretical value 633.21, found value 633.35.
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