Production method for lodixanol hydrolysate
A technology for iodixanol hydrolyzate and substance, which is applied in the preparation of organic compounds, the preparation of carboxylic acid amides, chemical instruments and methods, etc., can solve the problem of low yield, reduced reaction yield, difficult scale industrial production, etc problems, to achieve the effect of improving yield, reducing environmental pollution, and simplifying production operations
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Embodiment 1
[0033] In a 1000 ml reaction flask, add 59.9 g (0.1 mol) of 5-acetylamino-2,4,6-triiodo-1,3-benzenedicarboxamide, 16.6 g (0.15 mol, 13.6 ml) of α-chloroglycerol , a catalytic amount of pyridine, 300 milliliters of 1-butyl-3-methylimidazolium tetrafluoroborate, heated up to 100 ° C, stirred, and reacted for 4 hours. After the reaction was completed, cooled to room temperature and post-treated to obtain 67 grams of the product. Yield 90%.
Embodiment 2
[0035] In a 1000 ml reaction flask, add 59.9 g (0.1 mol) of 5-acetylamino-2,4,6-triiodo-1,3-benzenedicarboxamide, 11 g (0.1 mol, 9 ml) of α-chloroglycerol , a catalytic amount of triethylamine, 300 ml of 1-butyl-3-methylimidazolium tetrafluoroborate, heated up to 100°C, stirred, and reacted for 4 hours. After the reaction was completed, cooled to room temperature and post-processed to obtain the product 62 grams, yield 83%.
Embodiment 3
[0037] In a 1000 ml reaction flask, add 59.9 g (0.1 mol) of 5-acetylamino-2,4,6-triiodo-1,3-benzenedicarboxamide, 16.6 g (0.15 mol, 13.6 ml) of α-chloroglycerol , a catalytic amount of pyridine, using 300 ml of 1-butyl-3-methylimidazolium tetrafluoroborate, heated up to 100 ° C, stirred, and reacted for 4 hours. After the reaction was completed, cooled to room temperature and post-processed to obtain the product 67 grams, yield 90%.
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