Novel organic electroluminescent element compound and organic electroluminescent element comprising same
An electroluminescent device and compound technology, applied in the field of compounds for organic electroluminescent devices, can solve the problems of no electron transport ability, hole transport ability, thermal properties, etc.
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[0102] Example 1: Synthesis of Compound 1
preparation example 1
[0103] (1) Preparation Example 1: Synthesis of Intermediate Product 1-1
[0104]
[0105]In 1,2-diiodobenzene (1,2-diiodobenzene) (19.8g, 0.06mol, sigma aldrich), triisopropyl borate (16.9g, 0.09mol, sigma aldrich) Derich), catalyst CuI (1.14g, 0.006mol, Sigma-Aldrich), sodium hydride (sodium hydride) (2.2g, 0.09mol, Sigma-Aldrich) were added 800ml of THF, and stirred at 25°C for 12 hours. make it react. After completion of the reaction, distilled water was added for extraction and column purification (n-Hexane: methylene chloride) was performed to obtain 15.3 g (yield 77%) of intermediate product 1-1.
[0106] LC / MS: m / z=331[(M+1) + ]
preparation example 1-2
[0107] (2) Preparation Example 1-2: Synthesis of Intermediate Product 1-2
[0108]
[0109] In the intermediate product 1-1 (15.3g, 0.046mol), 1-iodo-2-nitrobenzene (1-iodo-2-nitrobenzene) (7.5g, 0.03mol, Sigma-Aldrich), Pd(Oac) 2 (0.34g, 0.0015mol, Sigma-Aldrich), P(tBu) 2 Me (0.48 g, 0.003 mol, Sigma-Aldrich) and KOtBu (10.1 g, 0.09 mol, Sigma-Aldrich) were added with 600 ml of t-Butyl alcohol, and the mixture was stirred at 25°C to make it reaction. After completion of the reaction, distilled water was added for extraction, and column purification (n-hexane:dichloromethane) was performed to obtain 8.5 g (yield 57%) of intermediate product 1-2.
[0110] LC / MS: m / z=325[(M+1) + ]
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