Colorant compound and coloring composition containing it
A technology for coloring compositions and compounds, which is applied in the direction of photoengraving process, isoindoline dyes, instruments, etc. of pattern surface, can solve the problems of difficulty in manufacturing film color filters, difficulty in increasing the pigment content of photosensitive resin compositions, and the like, Achieves stable color reproducibility, excellent heat resistance and solubility, and reduced usage
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preparation example 1
[0190] Preparation Example 1: Synthesis of Compound 1
[0191]
[0192] Compound A was obtained according to the method described in US Patent Publication No. 6849116 B2. In detail, 25.5 g of phthalimide and 7.4 g of paraformaldehyde were mixed and added to 560 g of 3.6% by weight of oleum at 25°C. The mixture was heated to 50°C and stirred for 30 minutes.
[0193] 100 g of Pigment Yellow 138 (BASF) was added thereto, and the mixture was heated to 100° C. and stirred for 3 hours. Subsequently, the mixture was added to 3500 g of water, and stirred at 60° C. for 30 minutes. The precipitated product thus obtained was filtered and washed with water until the product became neutral, and then dried in a vacuum oven at 90° C. to obtain compound (A).
[0194] Next, 3g (3.417mmol) compound (A), 0.52g (7.033mmol) 1-butanethiol and 1.94g (14.06mmol) K 2 CO 3 Place in 500ml single neck RBF and stir at 60°C for 24 hours. The reaction solution was cooled to room temperature, and ...
preparation example 2
[0195] Preparation Example 2: Synthesis of Compound 2
[0196]
[0197] Compound B was obtained according to the method described in US Patent Publication No. 6849116 B2 in the same manner as in Preparation Example 1, except that 1,8-naphthalimide was used instead of phthalimide.
[0198] Next, 3g (3.32mmol) compound (B), 0.49g (6.65mmol) 1-butanethiol and 1.83g (13.28mmol) K 2 CO 3 Place in 500ml single neck RBF and stir at 60°C for 24 hours. The reaction solution was cooled to room temperature, and filtered under reduced pressure. The solvent was removed under reduced pressure, and the resultant was purified by column to obtain compound 2. APCI negative MS analysis results showed that the molecular weight of compound 2 was 957.
preparation example 3
[0199] Preparation Example 3: Synthesis of Compound 3
[0200]
[0201] Compound C was obtained according to the synthesis method described in Korean Patent Publication No. 2013-0137028, and then Compound D was obtained according to the method described in US Patent Publication No. 6849116 B2.
[0202] Next, 3g (3.92mmol) compound (D), 0.58g (7.84mmol) 1-butanethiol and 2.17g (15.69mmol) K 2 CO 3 Place in 500ml single neck RBF and stir at 60°C for 24 hours. The reaction solution was cooled to room temperature, and filtered under reduced pressure. The solvent was removed under reduced pressure, and the resultant was purified by column to obtain compound 3. APCI negative MS analysis results showed that the molecular weight of compound 3 was 819.
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