A process for preparation of an aromatic n-glycidylamine
a technology of nglycidylamine and glycidylamine, which is applied in the field of preparation of aromatic nglycidylamine, can solve the problems of adversely affecting the properties of cured resins, unsuitable for industrial production of aromatic n, etc., and achieve the effect of facilitating dehydrochlorination
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[0025]Example 1: Bis(4-aminophenyl) methane, toluene and 50% lanthanum nitrate in 2-butoxyethanol are stirred and heated to 60 to 70° C. under a reduced pressure (200-400 mbar) followed by addition of epichlorohydrin over a period of 2 to 5 hours. After completion of epichlorohydrin addition, the mixture is maintained at 60 to 70° C. and then vacuum is released. A further portion of catalyst solution is added and the temperature is raised to 75 to 85° C. under reduced pressure. The mixture is then maintained under this condition for about 3 to 5 hours under constant stirring. The temperature is reduced to 60 to 70° C. and 50% aqueous benzyltrimethylammonium chloride is then added and the apparatus is set up for vacuum azeotrope. 50% aqueous sodium hydroxide is then added over a period of 1 to 3 hours, water being azeotroped out under vacuum (200-500 mbar). At the end of addition, azeotrope is continued for a further of 2 to 3 hours. Toluene and water are then added with stirring and...
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