Process for preparing disperse red 60
A production method and technology of disperse red, applied in the direction of amino-hydroxyanthraquinone dyes, etc., can solve the problems of shortening the condensation reaction time, lowering the condensation reaction temperature, etc., and achieve the effect of meeting the requirements of clean production, reducing dosage and reducing production cost
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Embodiment 1
[0025] Add 60 grams of dry product of 1-amino-2-bromo-4-hydroxyanthraquinone, 100 grams of phenol, 180 grams of nitrobenzene and 20 grams of potassium carbonate to the reaction kettle, and keep it warm for 7 to 9 hours at 155 ° C. After the end point is reached, excess phenol is removed by vacuum distillation. After the phenol is removed, it is cooled to 40°C, filtered with suction, and the mother liquor is reserved for the next batch. The filter cake was boiled with water to recover the solvent nitrobenzene. After the nitrobenzene was recovered, it was suction-filtered, drained, washed with a small amount of water, and dried to obtain 54.5 grams of a dry filter cake, which was Disperse Red 60, and the calculated yield was 89.7%.
Embodiment 2
[0027] Add 60 grams of 1-amino-2-bromo-4-hydroxyanthraquinone dry product, 100 grams of phenol, 180 grams of No. 200 solvent naphtha, and 20 grams of potassium carbonate to the reaction kettle, and keep the temperature at 155°C for 7 to 9 hours. After the measurement end point is reached, the excess phenol is removed by vacuum distillation. After the phenol is removed, it is cooled to 40°C, filtered with suction, and the mother liquor is reserved for the next batch. The filter cake was boiled with water to recover the solvent nitrobenzene. After the recovery of the nitrobenzene, it was suction-filtered, drained, washed with a small amount of water, and dried to obtain 53.8 grams of a dry filter cake, which was Disperse Red 60, and the calculated yield was 89.7%.
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