Aromatic diamines monomer with double miscellaneous naphthalenone structures and trifluoromethyl substituted and preparation thereof
A technology of trifluoromethyl and aromatic diamines, which is applied in the field of aromatic diamines and its preparation, can solve the problems of polyimide insolubility, loss, and reduction of high temperature resistance of polyimide, and achieve good film formation properties, excellent mechanical properties, and excellent heat resistance
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[0023] 2-(4-amino-2-trifluoromethylphenyl)-4-[4-(4-amino-2-trifluoromethylphenoxy)-naphthyl]-naphthyridine-1 - Preparation of ketones:
[0024] ①Under nitrogen protection, mix 22.9g (0.05mol) 4,4'-oxo-bis[(4-(1,4-phenyl)-phthalazin-1-one] and 22.6g (0.1mol) 2-Chloro-5-nitrobenzotrifluoride was added to a 500ml three-necked flask, and then 14.5g (0.105mol) of potassium carbonate and 150ml of N,N-dimethylformamide were added respectively, and the reaction was carried out at 100-150°C for 10- After 20 hours, the product was poured into 1000ml of methanol / water (1:1), fully stirred, precipitated and filtered, and the product was repeatedly washed with hot water, and further separated and purified by column chromatography to obtain a white fluorine-containing dinitro compound: 4,4'- Bis[2-(4-nitro-2-trifluoromethylphenyl)-phthalazin-1-one-yl]-diphenyl ether, the yield is about 70-80%, and the melting point is 159-161 ° C. FT -IR(KBr)v / cm -1 : 1677 (C=O), 1537, 1355 (-NO 2 ), 12...
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