Orange disperse dye monomeric compound and preparation method and application thereof
A technology of disperse dyes and compounds, applied in the field of non-ionic dyes, which can solve the problems of ineffective printing and dyeing and meet the requirements, and achieve the effects of low cost, good reproducibility, and simple preparation process
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Embodiment 1
[0024] The reaction equation is as follows:
[0025]
[0026] (1) Mix 17.6 g of the compound of formula (V), 40 ml of hydrogen peroxide, 23 ml of hydrobromic acid solution and 50 ml of water, and stir at room temperature for 8 hours to obtain the compound of formula (IV).
[0027] (2) Mix 15g of the compound of formula (IV), 15g of nitrosyl sulfuric acid and 45g of sulfuric acid, heat up to 30°C and stir for 2 hours. After the reaction is complete, add sulfamic acid for treatment to obtain the diazo compound shown in formula (III) liquid.
[0028] (3) Add 200g of ice to the above-mentioned diazotization solution, stir, slowly add 12g of the compound of formula (II) below 5°C, stir and react for 2 hours below 5°C, filter, wash with water, and dry to obtain 22.5g of the compound of formula (I) ) compound shown. Melting point: 195°C. H1-NMR (deuterated DMSO) spectrum see figure 1 .
Embodiment 2
[0030] Mix 40 g of the compound of formula (I) and 60 g of MF with water, grind and disperse with a grinder, and then spray dry to obtain an orange dye.
Embodiment 3
[0032] Take 2.0g of the disperse dyes prepared in Example 2, and use water to make disperse dye suspensions with a concentration of 2g / L, mix 2ml with 8ml of water, adjust the pH of the dyeing bath to 5 with acetic acid, and then heat up to 60°C , and at the same time put 2g of the fiber materials shown in the table below for high-temperature and high-pressure dyeing, heat up to 130°C within 30 minutes, keep warm for 30 minutes, cool down, and take samples. Check the infection rate. And test the rubbing resistance, washing resistance, sunlight resistance and sublimation fastness of Example 2 respectively according to the relevant provisions of the national standard.
[0033] As shown in the following table, the disperse dyes prepared by the compounds of the present invention are significantly better than the prior art in fastness to rubbing, washing, sunlight and sublimation.
[0034] Table 1
[0035]
[0036] Table 2
[0037]
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