Monoazo compounds, preparation method and uses thereof
A monoazo, compound technology, applied in the field of monoazo compounds, achieves the effects of good washing fastness, good sublimation fastness and good moisture resistance
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Embodiment 1
[0035] 2,4-dinitro-6-bromoaniline shown in formula (2)
[0036]
[0037] Carry out diazotization with nitrosyl sulfuric acid in sulfuric acid medium, the diazonium salt that obtains is coupled with the compound shown in formula (3) in acidic medium,
[0038]
[0039] where R 1 , R 2 , R 3 , R 4 and R 5 With the definition of the above-mentioned formula (1), then the obtained coupled compound is reacted with CuCN or NaCN+CuCN in an organic solvent to replace the bromine substituent, and the monoazo compound of the present invention shown in the formula (1) is obtained. compound.
[0040]
[0041] The diazo component (2) is known and readily available commercially, and the coupling component (3) can be prepared by well-known methods.
[0042] The present invention also relates to a mixture containing at least two azo compounds of different structures of the formula (1), which has better application properties. The mixture of the present invention can be prepared ...
Embodiment 2
[0045] Put 66.0ml of sulfuric acid into the flask, add 52.4g of 2,4-dinitro-6-bromoaniline at controlled room temperature, continue to stir for 30 minutes, cool with ice bath to reach 20-30°C, at this temperature 68.0g 42% nitrosyl sulfuric acid was added dropwise to the reaction mixture, and stirring was continued at this temperature for 4 hours. After completing the reaction, the mixture was dropped into a mixture of 30.0ml sulfuric acid, 900.0g ice water and 56.0g of the compound of the following formula within 30 minutes at 0-5°C,
[0046]
[0047] Stirring was continued for 2 hrs, then 1000 ml of water was added, and the temperature was slowly raised to 60° C. over 1 hour and kept for 1 hr. The resulting suspension was suction filtered, washed with water and dried.
[0048] A dye of the formula is obtained,
[0049]
[0050] Stir and mix 55.0g dry product of the above formula (4), 9.8g cuprous cyanide and 300g DMF, slowly raise the temperature to 60°C in 1 hour an...
Embodiment 3
[0055] Put 66.0ml of sulfuric acid into the flask, add 52.4g of 2,4-dinitro-6-bromoaniline under the control room temperature, continue to stir for 30 minutes, cool with ice bath to reach 20-30 ℃, under this temperature, 68.0 The 42% nitrosyl sulfuric acid of g is dripped in the reaction mixture, continues to stir at this temperature 4 hours.After completing the reaction, in 30 minutes, this mixture is dripped by 30.0ml sulfuric acid, 900.0g ice In the mixture of water and 50.5g following formula compound,
[0056]
[0057] Stirring was continued for 2 hrs, then 1000 ml of water was added, and the temperature was slowly raised to 60° C. over 1 hour and kept for 1 hr. The resulting suspension was suction filtered, washed with water and dried.
[0058] A dye of the formula is obtained,
[0059]
[0060]Stir and mix 52.6g of the dry product of the above formula (4b), 9.8g of cuprous cyanide and 300g of DMF, slowly heat up to 60°C in 1 hour and keep warm for 2hr, TLC test,...
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