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Vinyl caprolactam preparation method

The technology of vinyl caprolactam and base caprolactam is applied in the field of preparation of crystalline products and vinyl caprolactam, which can solve the problems of easily occurring correlative reactions, high technical difficulty, many side reactions, etc., so as to solve the problem of catalyst decomposition and deactivation, simplifying The effect of preparation process conditions

Active Publication Date: 2017-07-14
重庆晶粒化工有限公司
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

There are following problems in this synthesis process route: (1) prepare catalyst caprolactam potassium salt with caprolactam and alkali metal hydroxide, then potassium salt is added in the reaction system and react, because catalyst potassium salt encounters water or air will quickly Hydrolysis has only a short lifespan, and the presence of water will also lead to the ring opening of the raw material caprolactam, and the preparation of the catalyst caprolactam potassium salt in stages cannot solve the problem of easy deactivation of the catalyst
(2) It is reported in the literature that potassium tert-butoxide or cocatalyst crown ether is used to solve the problem in (1), but because of the high price, it only stays in the experimental stage and cannot realize large-scale industrial production
(3) According to literature reports, conventional stirred reactors are used, and the reaction conditions are either high pressure 4-12MPa, or high temperature 170-300°C, which is dangerous to operate and technically difficult.
Under high pressure and high temperature conditions, the reactor transmission and shaft rotation seals are prone to leakage, especially the leakage of acetylene gas will cause serious consequences and affect the surrounding environment
(4) Special reactors such as loop jet reactors are only in the experimental stage and cannot be industrialized yet.
(5) The process conditions for the preparation of vinyl caprolactam by the acetylene liquid phase addition method reported in the literature are still in the small-scale test stage, the reaction conditions are extreme, the reaction system is viscous and easy to solidify, and the product yield is generally low
[0006] At the same time, the vinyl caprolactam products reported in the literature are mainly purified by rectification tower purification, and the purification process has the following problems: (1) high equipment investment cost
(2) It is difficult to obtain high-purity vinyl caprolactam in one rectification
(4) There are catalysts and unreacted raw material caprolactam in the reaction solution at the same time. Under high temperature and alkaline conditions, caprolactam is easy to ring-open and polymerize, resulting in many side reactions in the rectification process, which are prone to correlative reactions and affect product yield.
(5) The product obtained after rectification is easy to form large massive crystals when stored at room temperature, and needs to be heated at a high temperature above 200°C to be melted and used. The melting process is likely to cause polymerization and discoloration of the product, which is not conducive to large drum packaging and storage

Method used

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  • Vinyl caprolactam preparation method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0058] In a 3000ml four-necked bottle equipped with an electric stirrer, a vacuum distillation device, a thermometer, and a vent valve, add 400g of caprolactam and 12g of potassium hydroxide for vacuum distillation, heat and melt for dehydration, the dehydration temperature is 80-150°C, and the time is 30- 90min, vacuum degree -0.01 to -0.085MPa, until no liquid drops flow out, forming a nucleophilic addition reaction system.

[0059] Continuously feed acetylene into the above system to carry out vinylation addition reaction. The set reaction temperature is 120°C, and the set temperature change is controlled in the reactor so that the set temperature change is controlled between 120±5°C and the pressure is 0-0.01MPa. The ventilation volume of acetylene is 0.0786m 3 , the ventilation rate is 160ml / min. When the ventilation is continued for 20 minutes, the temperature of the system continues to drop below 90°C, and the pressure of the system continues to rise above 0.01MPa, it...

Embodiment 2

[0063] Add 500g of caprolactam and 15g of potassium hydroxide to a 3000ml four-necked bottle equipped with an electric stirrer, a vacuum distillation device, a thermometer, and a vent valve, and heat and melt for dehydration. The dehydration temperature is 100-150°C and the time is 60-90min. , Vacuum degree -0.085 to -0.001MPa, until no liquid drops flow out, forming a nucleophilic addition reaction system.

[0064] Continuously feed acetylene into the above system to carry out vinylation addition reaction. The set reaction temperature is 100°C, and the set temperature change is controlled in the reactor so that the set temperature change is controlled between 100±5°C and the pressure is 0-0.025MPa. The ventilation volume of acetylene is 0.0983m 3 , the ventilation rate is 102ml / min. When the ventilation is continued for 25 minutes, the temperature of the system continues to drop below 90°C, and the pressure of the system continues to rise above 0.025 MPa, it is the end of t...

Embodiment 3

[0072] Preliminary purification product sample 1#, final purification product sample 1* and vinyl caprolactam sample 1 in comparative example 1 in Example 1 △ , to conduct relevant performance tests. The specific data results are shown in Table 1.

[0073] Table 1 Performance test results comparison table

[0074]

[0075] It can be seen from Table 1 that the product purity of the preliminary purified product sample and the final purified product sample prepared in Example 1 are ≥95% and ≥99% respectively, which are better than the vinylcaprolactam sample prepared in Comparative Example 1. At the same time, the final purified product sample prepared in Example 1 is a white or light yellow transparent liquid. Compared with the solid sample prepared in Comparative Example 1, no block crystals are formed, which is more convenient for packaging, storage, and use. Moreover, the sample prepared in Example 1 has a lower melting point than Comparative Example 1, which can meet th...

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Abstract

The invention discloses a vinyl caprolactam preparation method, and belongs to the technical field of chemical industry production. According to the present invention, based on the nucleophilic addition reaction principle, vinyl caprolactam is subjected to low temperature synthesis through a one-pot method by using an alkali metal salt or alkali metal hydroxide as a catalyst and using acetylene and caprolactam as raw materials, and then the vinyl caprolactam having different purities is obtained through polar solvent recrystallization and vacuum distillation; and the preparation method has characteristics of simple process, simple operation, mild and controlled reaction condition, reaction conversion rate improving, product yield improving and production cost reducing, effectively solves the problem of catalyst decomposition deactivation caused by the presence of the water in the system, avoids the occurrence of the side reaction, and avoids the pollution of the organic solvent on the environment, and the obtained two products such as the crystal and the liquid have different appearance forms and different purities so as to conveniently package and use.

Description

technical field [0001] The invention belongs to the technical field of chemical production, and relates to a preparation method of vinyl caprolactam, in particular to a preparation method of vinyl caprolactam and obtained crystal products of different forms. Background technique [0002] Vinyl caprolactam (N-Vinyl Caprolactam), CAS: 2235-00-9, the Chinese name is also called N-vinyl caprolactam, 1-vinyl hexahydro-2H-Y heptin-2-one, etc. The English name is also called vinyl caprolactam, 1-ethenylhexahydro-2H-Azrpin-2-one, vinyl-epsilon-caprolactam, etc. Its structural formula is as follows: [0003] [0004] Vinyl caprolactam is an important intermediate for the synthesis of poly-N-vinyl caprolactam. Poly N-vinylcaprolactam (PNVCL) is a temperature-sensitive high polymer with a low critical phase transition temperature (LCST). Its series of high polymers have extremely wide application prospects in biomedicine, daily chemicals, and petrochemicals. Therefore, the devel...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D223/10
CPCY02P20/52C07D223/10C07B2200/13
Inventor 汪帅汪叶舟刘茵
Owner 重庆晶粒化工有限公司
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