A kind of synthetic method of the dye intermediate with n-acetate group structure

The technology of a dye intermediate and a synthesis method is applied in the synthesis field of the dye intermediate, and can solve the problems of low reaction temperature, difficulty in recovery and reuse, large proportion of methyl chloroacetate and the like

Active Publication Date: 2021-09-14
湖南天童环保有限公司
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

For example, Chinese patent (CN106565528A) discloses that benzene-based solvents are used as water-carrying agents, organic amines are used as acid-binding agents, and aromatic amines and methyl chloroacetate are subjected to N-alkylation reactions. This method has a low reaction temperature and a long time, and is applicable to Synthesize dye intermediates with a monoacetate structure, the resulting dye intermediates containing methyl monoacetate have a purity of 96%, but for dye intermediates with a diacetate structure, as well as ethyl acetate, acetic acid The dye intermediate of propyl ester group has no embodiment report
Chinese patent (CN 102633666A) is aimed at the current containing methyl acetate group (-CH 2 COOCH 3 ) of the substituted aniline dye intermediates in the synthesis process requires a large proportion of methyl chloroacetate, difficulty in recycling, and easy deterioration in storage. N-alkylation reaction with methyl chloroacetate at reflux temperature to synthesize dye intermediate with diacetate structure
However, the reaction time of these techniques is longer, generally about 8 hours, and the resulting dye intermediate purity containing diacetate group is about 96% (HPLC), and there is no synthetic dye intermediate containing ethyl acetate group The example report
There is no literature report that can obtain more than 99% high-purity N,N-diacetate-based dye intermediates

Method used

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  • A kind of synthetic method of the dye intermediate with n-acetate group structure
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  • A kind of synthetic method of the dye intermediate with n-acetate group structure

Examples

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Embodiment 1

[0029] Synthesis of 2-methoxy-5-acetylamino-N,N-bis(ethyl acetate)aniline

[0030]In a 250mL three-necked flask with a stirrer, a thermometer and a reflux condenser (with a water separator), add 100.0 g of ethyl chloroacetate, 36.0 g of 2-methoxy-5-acetamidoaniline, and 23.2 g of sodium carbonate. Mix evenly under stirring, heat up to 90-105°C for reflux reaction for 2.0 hours; then add 3.0g of catalyst and 0.20g of zinc powder, heat up to 105-120°C, and carry out water separation and reflux reaction for 3.0h. Samples were taken and the purity of the target product was tested by high pressure liquid chromatography. After recovering ethyl chloroacetate by distillation under reduced pressure, add acetic acid to obtain an acetic acid solution containing 2-methoxy-5-acetylamino-N,N-bis(ethyl acetate)aniline, measure the coupling value, and calculate the yield . The results are shown in Table 1.

[0031] Table 1: Purity and Yield List of Synthesized Products Using Four Kinds of ...

Embodiment 2

[0038] Synthesis of m-Acetamido-N,N-bis(methylacetate)aniline

[0039] In a 250mL three-neck flask with a stirrer, a thermometer and a reflux condenser (with a water separator), add 108.5g of methyl chloroacetate, 30.0g of m-acetamidoaniline, and 23.2g of sodium carbonate, mix well under stirring, and heat up to Reflux reaction at 90-100°C for 2.0h; then add 2.0g of sodium bromide and 0.30g of zinc powder, raise the temperature to 105-110°C, and carry out water-dividing reflux reaction for 2.0h. Sampling was carried out and detected by high-pressure liquid chromatography. The purity of the main component m-acetamido-N,N-di(acetoxymethyl)aniline was 99.4%. After recovery of methyl chloroacetate by vacuum distillation, acetic acid was added to obtain an acetic acid solution containing m-acetamido-N,N-di(acetoxymethyl)aniline. The yield was 98.6% by measuring the coupling value.

Embodiment 3

[0047] Synthesis of m-propionylamino-N,N-bis(ethyl acetate)aniline

[0048] In a 250mL three-necked flask equipped with a stirrer, a thermometer, and a reflux condenser (with a water trap), add 110.0 g of ethyl chloroacetate, add 33.0 g of m-propionamidoaniline, and 25.0 g of sodium carbonate under stirring. well mixed. Raise the temperature to 100-110°C, and reflux for 1.0h. Add 2.5g of sodium bromide and 0.25g of zinc powder, and reflux at 110-125°C for 3.0h. Sampling and detection by high-pressure liquid chromatography showed that the target product had a purity of 99.2%. After the ethyl chloroacetate was recovered by distillation under reduced pressure, acetic acid was added to obtain the acetic acid solution of m-propionylamino-N,N-bis(ethyl acetate)aniline, with a yield of 98.4%.

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Abstract

The invention discloses a method for synthesizing a dye intermediate with an N-acetate group structure. The method comprises reflux reaction of substituted aniline, chloroacetate and an acid-binding agent at a temperature of 80-110°C for 0.5-2.0 hours Finally, add catalyst and zinc powder, and further carry out water separation and reflux reaction at 105-130°C for 1.0-3.0 hours to obtain a dye intermediate; this dye intermediate can be directly used in dye synthesis, and the synthesis method has a catalytic reaction speed Fast, with a product purity of over 99% (HPLC), and a yield of over 98%. This method is especially suitable for the synthesis of dye intermediates containing N,N-diacetate groups with a purity of over 99%.

Description

technical field [0001] The invention relates to a synthesis method of a dye intermediate, in particular to a synthesis method of a dye intermediate with an N-acetate group structure, and belongs to the technical field of dyes. Background technique [0002] Aromatic amines substituted with N-ester groups are an important class of disperse dye intermediates, and there are mainly three synthetic methods. The first method is that the amino group of the aromatic amine is hydroxyethylated with ethylene oxide, and then esterified with acetic acid or acetic anhydride. For example, the coupling component of disperse blue 79 was synthesized from 2-methoxy-5-acetamidoaniline. The second method is that the amino group of the aromatic amine is obtained by addition of an alkylating agent containing a propionate group. For example, the addition reaction of 2-methoxy-5-acetamidoaniline and methyl acrylate, the addition reaction of aniline and methyl acrylate. The third method is that the...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C231/12C07C233/43C07C233/80
Inventor 赵莹胡仁杰熊远福赵起袁遥谭晓燕
Owner 湖南天童环保有限公司
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