an acid dye
A technology of acid dyes and compounds, applied in the direction of azo dyes, organic dyes, disazo dyes, etc., can solve the problems of poor light fastness and light fastness reduction of dyes
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preparation Embodiment 1
[0055] Add 15.0 parts of 4-aminoacetanilide to a mixture of 50 parts of ice and 25 parts of hydrochloric acid with a strength of about 30% by volume, and stir for about 30 minutes. At 0-5[deg.] C., 17.3 parts of a 40% by volume sodium nitrite solution were added dropwise within 30 minutes. The temperature was maintained at 0-5°C by adding ice during the addition. After the diazotization is complete, the excess sodium nitrite is destroyed with sulfamic acid.
[0056] 29.1 parts of 3-[(ethylphenylamino)methyl]benzenesulfonic acid were suspended in 200 parts of water. The pH of the suspension was adjusted to 7-7.5 with sodium carbonate. Under vigorous stirring, the diazo compound suspension was added within 30 minutes. During the addition, the pH was maintained at around 7 by metering in sodium carbonate solution.
[0057] After the coupling reaction is complete, 50 parts of an aqueous sodium hydroxide solution having a strength of about 30% by volume is added and the reactio...
preparation Embodiment 2-8
[0063] The following table contains the dyes prepared in a similar manner to that described in Example 1 by using the corresponding starting materials. These dyes wool (especially polyamide) blue with very good light and wet fastnesses. It can be seen from the data in the table that the compounds disclosed in the present invention have good light fastness, wet fastness and rubbing fastness. Compared with the compound disclosed in CN101479348A, it has significant improvement in light fastness and wet fastness.
[0064]
[0065]
[0066] Test method for light (sunlight) fastness: GB / T 8427-1998, 3% owf; test method for washing fastness: ISO1OS-C2S; test method for water fastness: GB / T 428-1978; perspiration fastness test Method: ISO 105 / E04-1994; Test method for rubbing fastness: GB 3920.
[0067] The comparative examples in the table are the compounds disclosed in CN 101479348A. Wherein, R1, R2, R6 in the comparative example in the table and the compound of the present...
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