Method for the synthesis of anthraquinone dye or chromophore by aryl amination of bromoacid
A bromamic acid arylamine, anthraquinone type technology, applied in the field of dyes, can solve the problems of reducing the amount of catalyst used and converting bromamic acid to COD, etc.
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Embodiment 1
[0050] Weigh 8.4 g of sodium 2,4-diaminobenzenesulfonate, 8.4 g of sodium bicarbonate, and 20 ml of water, add them into a container equipped with a stirrer, condenser, and thermometer, and heat to 80°C while stirring. Weigh respectively 8.08 grams of bromine, 15% mol (based on bromine) of monovalent copper and 1,4,7,10-tetraazacyclododecane-1,3-diene (C 8 h 18 N 4 ) complex aqueous solution. Alternately add solid bromine and monovalent copper complexes into the container within 1 hour, keep the reaction temperature at 80-82°C, the pH of the reaction system at 9, and stir for 3 hours; raise the reaction temperature to 85-90°C, stir Reaction, sampling for thin-layer chromatography and liquid chromatography analysis, no bromidine as the reaction end point. In the reaction liquid mixture, there are no hydrolyzed products of bromoacidic acid (purple side) and bicondensates, but there are traces of debrominated products.
[0051] The above materials were cooled to 40°C, slowly ...
Embodiment 2
[0053] Weigh 21 grams of 2,4-diaminobenzenesulfonic acid, 26.5 grams of sodium carbonate, and 50 milliliters of water, add them into a container equipped with a stirrer, a condenser, and a thermometer, and heat to 80°C while stirring. Weigh respectively 20.2 grams of bromine, 10% mol (based on bromine) of monovalent copper and 1,4,7,10-tetraazacyclododecane-1,3-diene (C 8 h 18 N 4 ) complex aqueous solution. Alternately add solid bromine and monovalent copper complexes into the container within 2.5 hours, keep the reaction temperature at 80-82°C, the pH of the reaction system at 9, and stir for 3 hours; raise the reaction temperature to 85-90°C, stir Reaction, sampling for thin-layer chromatography and liquid chromatography analysis, no bromidine as the reaction end point. In the reaction liquid mixture, there are no hydrolyzed products of bromoacidic acid (purple side) and bicondensates, but there are traces of debrominated products.
[0054] The above materials were cool...
Embodiment 3
[0056] Weigh 8.4 g of 2,4-diaminobenzenesulfonic acid, 8.4 g of sodium bicarbonate, and 20 ml of water, add them into a container equipped with a stirrer, a condenser, and a thermometer, and heat to 80°C while stirring. Weigh respectively 8.08 grams of bromine, 10% mol (based on bromine) of monovalent copper and 1,4,7,10-tetraazacyclododecane-1,3-diene (C 8 h 18 N 4 ) complex ethanol solution. Alternately add solid bromine and monovalent copper complexes into the container within 1 hour, keep the reaction temperature at 80-82°C, the pH of the reaction system at 9, and stir for 2 hours; raise the reaction temperature to 80-90°C, stir Reaction, sampling for thin-layer chromatography and liquid chromatography analysis, no bromidine as the reaction end point. In the reaction liquid mixture, there are no hydrolyzed products of bromoacidic acid (purple side) and bicondensates, but there are traces of debrominated products.
[0057] The above materials were cooled to 40°C, slowly...
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