Preparation method for melamine derivative
A technology of melamine and derivatives, applied in the direction of organic chemistry, etc., can solve the problems of inability to detect in time, use, store, transport trouble, restrict commercialization, etc., achieve simple and clear judgment method, convenient measurement and operation, and facilitate commercial use. Effect
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Embodiment 1
[0031] 5L four-necked flask, electric heating mantle, tail gas absorption device filled with sulfuric acid aqueous solution, condensation reflux device, distillation unit, vacuum pump Add 1260g melamine, 2026g diglycolamine, 126g diglycolamine and 5L four-necked flask Phosphoric acid, hypophosphorous acid complex, start stirring and heat up to 200°C, react under reflux, pass a weak nitrogen flow after 6 hours until the material is clear and transparent, take samples every 2 minutes and mix them with ethanol at a mass ratio of 1:5 until the first No precipitation occurred during sampling for 5 times, and 20 g of solid sodium hydroxide was added, and vacuum was opened to remove and collect unreacted diglycolamine. After the temperature of the material rose to 260°C, the heating was stopped, and the temperature was lowered to 150°C under stirring and nitrogen protection, and the material was released. After cooling, 2552.1g of a translucent white solid was obtained, with a fra...
Embodiment 2
[0033] Add 31.5kg of melamine, 50.65kg of diglycolamine, 3.15kg of diglycolamine, phosphoric acid, and hypophosphorous acid complex into a 200L reactor, start stirring and raise the temperature to 198°C, react under reflux, and pass it in after 6 hours Nitrogen until the material is clear and transparent, take a sample every 2 minutes and mix it with ethanol at a mass ratio of 1:5. No precipitation occurs at the 8th sampling, add 500g of solid sodium hydroxide, turn on vacuum to remove and collect unreacted diglycolamine . When the temperature of the material rose to 250° C., the heating was stopped, and the temperature was lowered to 150° C. under the protection of nitrogen, and the material was released to obtain 64.74 kg of light yellow solid and 14.41 kg of fractions. The average degree of substitution was 1.45 calculated from the material balance. The obtained product has a softening point of 70-75°C and a melting range of 100-110°C.
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