Novel compoundphotosensitive resin composition comprising the same and color filter
A compound and chemical formula technology, applied in the field of novel compounds, can solve problems such as the brightness and contrast ratio limitations of color filters
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Synthetic example 1
[0222] Synthesis Example 1: Synthesis of 4-(biphenyl-2-yloxy)-3,5,6-trichloro-phthalonitrile
[0223]5 grams of 3,4,5,6-tetrachlorophthalonitrile, 3.21 grams of 2-phenylphenol, 3.9 grams of K 2 CO 3 And 25 ml of acetone were placed in a 100 ml flask, and then stirred while heating at 70°C. When the reaction was complete, the resultant was filtered and washed with acetone, and the liquid obtained therefrom was distilled to obtain a solid. Herein, the obtained solid was dissolved in a small amount of dichloromethane, and then washed several times with hexane, filtered and dried under vacuum to obtain 4-(biphenyl-2-yloxy)-3,5,6 - Trichloro-phthalonitrile.
Synthetic example 2
[0224] Synthesis Example 2: Synthesis of 3,4,6-trichloro-5-(2,6-dichloro-phenoxy)-phthalonitrile
[0225] 5 grams of 3,4,5,6-tetrachlorophthalonitrile, 3.06 grams of 2,6-dichlorophenol, 3.9 grams of K 2 CO 3 And 25 ml of acetone were placed in a 100 ml flask, and then stirred while heating at 70°C. When the reaction was complete, the resultant was filtered and washed with acetone, and the liquid obtained therefrom was distilled to obtain a solid. Herein, the obtained solid was dissolved in a small amount of dichloromethane, and then washed several times with hexane, filtered and dried under vacuum to obtain 3,4,6-trichloro-5-(2,6-dichloro -phenoxy)-phthalonitrile.
Synthetic example 3
[0226] Synthesis Example 3: Synthesis of 3,4,6-trichloro-5-(2,6-dibromo-phenoxy)-phthalonitrile
[0227] 5 grams of 3,4,5,6-tetrachlorophthalonitrile, 4.75 grams of 2,6-dibromophenol, 3.9 grams of K 2 CO 3 and 25 ml of N,N-dimethylformamide were placed in a 100 ml flask, and stirred while heating at 70°C. When the reaction was complete, EA (ethyl acetate) was used for extraction. After extraction, the resultant was concentrated to obtain a solid. The obtained solid was dissolved in a small amount of dichloromethane, washed several times with hexane, filtered and dried in vacuo to obtain 3,4,6-trichloro-5-(2,6-dibromo-phenoxy)- Phthalonitrile.
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