Preparation method of permanent violet pigment
A technology of permanent violet and pigment, applied in the direction of bisazine oxazine dyes, etc., can solve the problems of low selectivity of closed-loop reaction, a large amount of by-product hydrochloric acid, a large amount of waste residue, etc., to improve the selectivity and total yield, reduce by-products, etc. The effect of generating and reducing environmental pollution
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Embodiment 1
[0022] Put 210g of 3-amino-N-ethylcarbazole and 2000ml of o-dichlorobenzene into a 5000ml reactor, stir and dissolve and heat up to 35°C, add 140.7g of tetrachlorobenzoquinone, then dropwise add 105g of triethylamine, and then Incubate at ℃ for 3 hours to obtain a solution containing 2,5-dichloro-3,6-bis(9-ethyl-3-carbazolylamino)-1,4-benzoquinone, add 1g of copper sulfate to the reactant and 2g of anthraquinone, close the reactor, feed oxygen, control the pressure at 0.2MPa, heat up to 165°C, maintain this temperature for 4 hours, the reaction is over, cool to 100°C, discharge, filter, and successively use o-dichlorobenzene , methanol and water, and dried to obtain 279.5g crude permanent violet pigment, with a yield of 94.9% and a content of 98.5%.
Embodiment 2
[0024] Put 210g of 3-amino-N-ethylcarbazole and 2000ml of o-dichlorobenzene into a 5000ml reactor, stir and dissolve and heat up to 36°C, add 140.7g of tetrachlorobenzoquinone, then dropwise add 105g of triethylamine, and then Incubate at ℃ for 3 hours to obtain a solution containing 2,5-dichloro-3,6-bis(9-ethyl-3-carbazolylamino)-1,4-benzoquinone, heat up to 150℃ under stirring, Add 140g of benzenesulfonyl chloride, continue to heat up to 178°C, and keep warm at this temperature for 4 hours. After the reaction is completed, cool to 130°C and discharge, filter, wash with o-dichlorobenzene, methanol and water in sequence, and dry to obtain 249.2g Solid purple pigment crude product, the yield is 84.6%, the content is 98.6%.
Embodiment 3
[0026] Put 210g of 3-amino-N-ethylcarbazole and 2000ml of o-dichlorobenzene into a 5000ml reactor, stir and dissolve and heat up to 37°C, add 140.7g of tetrachlorobenzoquinone, then dropwise add 105g of triethylamine, and then Incubate at ℃ for 3 hours to obtain a solution containing 2,5-dichloro-3,6-bis(9-ethyl-3-carbazolylamino)-1,4-benzoquinone, add 3g of copper sulfate to the reactant , close the reactor, feed oxygen, control the pressure at 0.2MPa, raise the temperature to 165°C, keep the temperature at this temperature for 4 hours, after the reaction is completed, cool to 100°C and discharge, filter, and use o-dichlorobenzene, methanol and water in sequence After washing and drying, 263.6g of crude permanent violet pigment was obtained, with a yield of 89.5% and a content of 97.8%.
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