Preparation and application of a kind of organic luminescent compound
An organic and luminescent technology, applied in the preparation of organic compounds, amino compounds, organic chemistry, etc., can solve the problems of complex synthesis methods, inability to meet industrialization, and difficulty in purification, and achieve high luminous efficiency
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Embodiment 1
[0022] Embodiment 1: the synthesis of compound 001
[0023] The specific synthetic route is shown in the figure below:
[0024]
[0025] (1) Under the condition of nitrogen protection, add 15ml of anhydrous tetrahydrofuran solution, 2.64g of magnesium bars, and 1 grain of iodine into the three-necked flask. 50ml of tetrahydrofuran solution in water was reacted for 3 hours in an ice-water bath, 8.5ml of anhydrous N,N-dimethylformamide was added dropwise to the reaction solution, and then slowly raised to room temperature, and the reaction was continued for 3 hours. After adding 1M hydrochloric acid and 100ml ethyl acetate for liquid separation and extraction, the organic layer was washed with distilled water and saturated brine, dried over sodium sulfate, concentrated, and the resulting crude product was subjected to column chromatography (cyclohexane / dichloromethane=2 / 1), the obtained liquid was rotary evaporated and dried, and as a result, 12.8 g of off-white solid 2,7-t...
Embodiment 2
[0028] Embodiment 2: the synthesis of compound 002
[0029] The specific synthetic route is shown in the figure below:
[0030]
[0031] (1) Under the condition of nitrogen protection, add 15ml of anhydrous tetrahydrofuran solution, 2.64g of magnesium bars, and 1 grain of iodine into the three-necked flask. 50ml of tetrahydrofuran solution in water was reacted for 3 hours in an ice-water bath, 8.5ml of anhydrous N,N-dimethylformamide was added dropwise to the reaction solution, and then slowly raised to room temperature, and the reaction was continued for 3 hours. After adding 1M hydrochloric acid and 100ml ethyl acetate for liquid separation and extraction, the organic layer was washed with distilled water and saturated brine, dried over sodium sulfate, concentrated, and the resulting crude product was subjected to column chromatography (cyclohexane / dichloromethane=2 / 1), the obtained liquid was rotary evaporated and dried, and as a result, 12.8 g of off-white solid 2,7-t...
Embodiment 3
[0034] Embodiment 3: the synthesis of compound 003
[0035] The specific synthetic route is shown in the figure below:
[0036]
[0037] (1) Under the condition of nitrogen protection, add 15ml of anhydrous tetrahydrofuran solution, 2.64g of magnesium bars, and 1 grain of iodine into the three-necked flask. 50ml of tetrahydrofuran solution in water was reacted for 3 hours in an ice-water bath, 8.5ml of anhydrous N,N-dimethylformamide was added dropwise to the reaction solution, and then slowly raised to room temperature, and the reaction was continued for 3 hours. After adding 1M hydrochloric acid and 100ml ethyl acetate for liquid separation and extraction, the organic layer was washed with distilled water and saturated brine, dried over sodium sulfate, concentrated, and the resulting crude product was subjected to column chromatography (cyclohexane / dichloromethane=2 / 1), the obtained liquid was rotary evaporated and dried, and as a result, 12.8 g of off-white solid 2,7-t...
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