Boron-containing organic compound and application thereof
An organic compound and selected technology, applied in the direction of organic chemistry, compounds containing elements of Group 3/13 of the periodic table, applications, etc., can solve the problems of reduced luminous efficiency, disadvantage of high brightness, etc., and achieve long life and improve luminous efficiency. and longevity, the effect of low roll-off
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Embodiment 1
[0160] The synthetic route of compound (1) is as follows:
[0161]
[0162] Synthesis of intermediates 1-3:
[0163] Under a nitrogen atmosphere, in a dry three-necked flask, respectively add 10mmol of intermediate 1-1 and 10mmol of intermediate 1-2, 0.2mmol of palladium acetate, 1.38 g of potassium carbonate, add 150ml of tetrahydrofuran to dissolve it, and heat to 80 ℃ to the reflux of the reaction solution, and reacted for 12 hours. After the reaction was complete, the reaction was extracted with water, and the organic phase was extracted with dichloromethane at the same time. , purified by flash column chromatography to obtain 6.93 mmol of intermediate 1-3, yield: 69.3%. MS (ASAP) = 341.8.
[0164] Synthesis of Intermediates 1-5:
[0165] Under nitrogen protection atmosphere, in a dry three-necked flask, add 1mmol of intermediate 1-3 and 1mmol of intermediate 1-4 respectively, pour 100ml of DMSO as a solvent, add dry K 2 CO 3 As a base, react at 120°C for 8 hours, ...
Embodiment 2
[0169] The synthetic route of compound (2) is as follows:
[0170]
[0171] Synthesis of Intermediate 2-3:
[0172] Under a nitrogen atmosphere, in a dry three-necked flask, respectively add 10mmol of intermediate 2-1 and 10mmol of intermediate 2-2, 0.2mmol of palladium acetate, 1.38 g of potassium carbonate, add 150ml of tetrahydrofuran to dissolve it, and heat to 80 ℃ to the reflux of the reaction solution, and reacted for 12 hours. After the reaction was complete, add water to extract the reaction, and at the same time extract the organic phase with dichloromethane, combine and wash the organic phase several times, dry with anhydrous magnesium sulfate, filter, and spin evaporate to dryness to obtain crude oil. , purified by flash column chromatography to obtain intermediate 2-3 with a molar weight of 8.17 mmol and a yield of 81.7%. MS (ASAP) = 722.7.
[0173] Synthesis of Intermediates 2-5:
[0174] Under nitrogen protection atmosphere, in a dry three-necked flask, ad...
Embodiment 3
[0178] The synthetic route of compound (3) is as follows:
[0179]
[0180] Synthesis of Intermediate 3-3:
[0181] Under nitrogen atmosphere, in a dry three-necked flask, respectively add 10mmol of intermediate 3-1 and 10mmol of intermediate 3-2, 0.2mmol of palladium acetate, 1.38 g of potassium carbonate, add 150ml of tetrahydrofuran to dissolve it, and heat to 80 ℃ to the reflux of the reaction solution, and reacted for 12 hours. After the reaction was complete, add water to extract the reaction, and at the same time extract the organic phase with dichloromethane, combine and wash the organic phase several times, dry with anhydrous magnesium sulfate, filter, and spin evaporate to dryness to obtain crude oil. , purified by flash column chromatography to obtain intermediate 3-3 with a molar weight of 8.81 mmol and a yield of 88.1%. MS (ASAP) = 952.3.
[0182] Synthesis of intermediates 3-5:
[0183] Under nitrogen protection atmosphere, in a dry three-necked flask, add ...
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