Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method of 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxynonane

A technology of triperoxynonane and trimethyl, applied in the field of organic synthesis, can solve the problems of reducing the stirring effect, reducing the effective contact of raw materials, increasing the processing capacity, etc., achieving a stable and safe production process, reducing the invalid processing capacity, and increasing the effective effect of contact

Active Publication Date: 2015-04-15
浙江绍风塑业有限公司
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] ①The presence of a large number of inert diluents and solvents reduces the concentration of raw materials. In order to achieve the desired synthesis effect, the input amount and concentration of raw materials must be increased, especially the use of high-concentration concentrated sulfuric acid and hydrogen peroxide, which is harmful to raw material storage and safe production. pose a major safety hazard
[0007] ②The reaction rate is reduced, the effective contact between raw materials is reduced, and the stirring effect is reduced. In order to achieve a high conversion rate, a longer reaction time is required, which greatly prolongs the reaction process
Due to the lengthening of the reaction time, the probability of various safety accidents is increased, the labor and energy consumption of personnel are increased, and the requirements for equipment are higher, which is not conducive to energy conservation and environmental protection.
[0008] ③The addition of a large amount of inert diluents and solvents increases the difficulty of removing by-products and impurities generated during synthesis, resulting in increased processing capacity and reduced processing effects, resulting in insufficient product purity and high impurity content
[0009] ④The inert diluent and solvent are added before the reaction. Due to the uncertainty of the reaction process, in order to ensure the active oxygen content of the organic peroxide in the finished product, a second deployment is required, resulting in material loss and energy consumption

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxynonane
  • Preparation method of 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxynonane
  • Preparation method of 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxynonane

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] The preparation method of 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxynonane is as follows:

[0043] (1) Add 70% hydrogen peroxide into the three-necked flask, and reduce the charging temperature to 20°C;

[0044] (2) Adjust the stirring speed to 100~200RPM, add 65% concentrated sulfuric acid dropwise to the three-necked flask, and maintain the temperature to 20°C;

[0045] (3) Under the same stirring speed, add the calculated amount of methyl ethyl ketone dropwise to the three-necked flask, so that the molar ratio of methyl ethyl ketone, hydrogen peroxide and concentrated sulfuric acid is 3:3:0.3, and the temperature is controlled to 20 ℃, timed reaction for 4 hours, warmed up to 30 ℃, continued to react for 2 hours, the reaction was finished, cooled to 20 ℃, stood still, and layered, and the organic layer was the semi-finished product;

[0046](4) Dropwise add metered 10% sodium hydroxide solution to the above organic layer, control the reaction temperature to 20°C...

Embodiment 2

[0050] The preparation method of 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxynonane is as follows:

[0051] (1) Add 20% hydrogen peroxide into the three-necked flask, and lower the feeding temperature to 30°C;

[0052] (2) Adjust the stirring speed to 100~200RPM, add 85% concentrated sulfuric acid dropwise into the three-necked flask, and keep the temperature at 30°C;

[0053] (3) At the same stirring speed, drop the calculated amount of methyl ethyl ketone into the three-necked flask so that the molar ratio of methyl ethyl ketone, hydrogen peroxide, and concentrated sulfuric acid is 3:3:0.5, and control the temperature to 30 °C, timed reaction for 3 hours, raised the temperature to 35 °C, and continued to react for 4 hours. After the reaction was completed, the temperature was lowered to 20 °C, left to stand, separated, and the organic layer was a semi-finished product;

[0054] (4) Use a metered 20% sodium hydroxide solution in the above organic layer, control the reactio...

Embodiment 3

[0058] The preparation method of 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxynonane is as follows:

[0059] (1) Add 50% hydrogen peroxide into the three-necked flask, and lower the feeding temperature to 10°C;

[0060] (2) Adjust the stirring speed to 100~200RPM, add 50% concentrated sulfuric acid dropwise into the three-necked flask, and keep the temperature at 10°C;

[0061] (3) At the same stirring speed, drop the calculated amount of methyl ethyl ketone into the three-necked flask so that the molar ratio of methyl ethyl ketone, hydrogen peroxide, and concentrated sulfuric acid is 3:3:1, and control the temperature to 10 °C, timed reaction for 2 hours, raised the temperature to 30 °C, continued to react for 3 hours, the reaction was completed, cooled to 20 °C, stood still, separated, the organic layer was a semi-finished product;

[0062] (4) Add dropwise and metered 30% sodium hydroxide solution to the above organic layer, control the reaction temperature to 10°C, react...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention belongs to the field of organic synthesis and discloses a preparation method of 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxynonane. The preparation method mainly comprises peroxidatic reaction, condensation polymerization reaction and a blending refining process and particularly comprises the following steps of: stirring concentrated sulfuric acid used as a catalyst as well as hydrogen peroxide and methyl ethyl ketone used as raw materials at the temperature condition of 10-50 DEG C for reacting for 0.5-6.0h, then cooling to 20 DEG C, standing for layering, and retaining an organic layer, wherein the molar ratio of the methyl ethyl ketone to the hydrogen peroxide to the concentrated sulfuric acid is 3:(1-6):(0.3-3); neutralizing the reaction solution with aqueous alkali with the concentration of 10-50% in the organic layer, carrying out washing refining, removing byproducts, after the reaction, standing, cooling, separating the solution, drying, and filtering to obtain a pure target product; and adding a diluent to obtain a finished product. The preparation method disclosed by the invention is simple in reaction process, higher in yield, safe and environment-friendly.

Description

technical field [0001] The invention belongs to the field of organic synthesis, and particularly relates to a preparation method of 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxynonane. Background technique [0002] Organic peroxides are a class of important and special chemical substances with strong oxidizing properties. The peroxy bonds (-O-O-) in organic peroxide molecules are easily decomposed into active radicals and oxygen when heated. It has the ability to release free radicals, so it is widely used in polypropylene, polyethylene, polyvinyl chloride, polystyrene, polyester, synthetic resin, synthetic rubber and other industries and other industries. Radical polymerization is an efficient method for large-scale production of various olefinic polymers. The advantages of free radical polymerization are that there are many kinds of polymerizable monomers, the reaction conditions are mild and easy to control, and it is easy to realize industrial production. More than 70...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C07D323/00
Inventor 吴洋董昆娟喻瑶夏少伟董志烽
Owner 浙江绍风塑业有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products