Bi(N-methylphthalic imidine) ester preparation method
A technology of methyl phthalimide and nitro phthalimide, applied in the field of bis-ether preparation, can solve problems such as high cost, difficulty in popularization and application, and large amount of three wastes to be treated, and achieves The effect of low production cost, easy recycling and low environmental pollution
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Embodiment 1
[0016] Add 206 gram (1mol) N-methyl-4-nitrophthalimide and composite catalyst in 1000ml (three-necked flask) equipped with stirrer, condenser, thermometer: 63.6 gram (0.6mol) sodium carbonate , 16.2 grams (0.27mol) of fumed white carbon black, 8.05 grams (0.025mol) of tetrabutylammonium bromide and 270ml dimethyl sulfoxide, heated and stirred to reflux, after 6 hours, the reaction ended, filtered while hot, and the filtrate was cooled After reaching room temperature, the product was precipitated. After filtering, recovering the solvent, washing with water and drying, 127 grams of brown-yellow bis(N-methylphthalimide) ether product was obtained, with a yield of 75.6% and a melting point of 268.5 to 271° C.
Embodiment 2
[0018] With embodiment 1, add composite catalyst and be: 74.2 grams (0.7mol) sodium carbonate, fumed white carbon black 14.7 grams (0.245mol), tetrabutylammonium bromide 14.49 grams (0.045mol) reacted 8 hours. Other conditions are identical with embodiment 1. 133 g of brown-yellow bis(N-methylphthalimide) ether was obtained with a yield of 79.2% and a melting point of 269-271°C.
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