A method for synthesizing aminopyridine from pyridine base mixture and its separation and purification method

An aminopyridine and mixture technology, which is applied to the synthesis of chemical intermediates and the synthesis of aminopyridines from pyridine base mixtures, can solve problems such as difficult separation of mixtures, and achieve the effects of avoiding environmental pollution, high income and low cost.

Active Publication Date: 2017-05-17
ANHUI XINGYU CHEM
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Aiming at the problem that the mixture of 2-picoline, pyridine and 4-picoline is difficult to separate in the prior art, the present invention provides a method for synthesizing aminopyridine from a mixture of pyridine bases and a separation and purification method thereof. The mixture is reacted with sodium amide under suitable conditions, and then the hydrolysis reaction is carried out to obtain the mixture of 2-amino-4-picoline, 2-aminopyridine and 2-amino-6-picoline, according to the composition of each component in the mixture The melting point and boiling point are different, and 2-amino-4-picoline, 2-aminopyridine and 2-amino-6-picoline are separated one by one to obtain high-purity 2-amino-4-picoline, 2-amino Pyridine and 2-amino-6-methylpyridine

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
  • A method for synthesizing aminopyridine from pyridine base mixture and its separation and purification method
  • A method for synthesizing aminopyridine from pyridine base mixture and its separation and purification method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Such as figure 1 Shown, a kind of method is synthesized aminopyridine by pyridine base mixture, and its step is:

[0038] (a) Xylene (does not contain ferric ion and water) is added in the reaction flask, then the pyridine base mixture that is made up of 2-picoline, pyridine and 4-picoline is added in the reaction flask through a constant pressure funnel and stirred evenly, Wherein the mass ratio of xylene to the pyridine base mixture is 2.5:1, 2-picoline accounts for 90% of the total mass, pyridine is 6%, and 4-picoline is 4% in the pyridine base mixture;

[0039] (b) Slowly heating the reaction flask in step (a) to 80° C. for reflux dehydration until no water droplets are generated in the reaction flask;

[0040] (c) After the dehydration reaction in step (b) is finished, it is cooled to room temperature, and sodium amide is added (addition speed is 10g / min) into the reaction flask and stirred evenly, and then micro-reflux reaction is carried out, wherein sodium amid...

Embodiment 2

[0051] A method for synthesizing aminopyridine from a pyridine base mixture, the steps are:

[0052] (a) Xylene (does not contain iron ion) is added in the reaction flask, then the pyridine base mixture that is made up of 2-picoline, pyridine and 4-picoline is added in the reaction flask through a constant pressure funnel and stirred evenly, wherein two The mass ratio of toluene to the pyridine base mixture is 2:1, and in the pyridine base mixture, 2-picoline accounts for 82% of the total mass, pyridine is 11%, and 4-picoline is 7%;

[0053] (b) Slowly heating the reaction flask in step (a) to 100° C. for reflux dehydration until no water droplets are generated in the reaction flask;

[0054] (c) After the dehydration reaction in step (b) is finished, it is cooled to room temperature, and sodium amide is added in the reaction flask with a speed of 15g / min and stirred evenly, and then micro-reflux reaction is carried out, wherein the mass of sodium amide and pyridine base mixtu...

Embodiment 3

[0065] A method for synthesizing aminopyridine from a pyridine base mixture, the steps are:

[0066] (a) Xylene (does not contain iron ion) is added in the reaction flask, then the pyridine base mixture that is made up of 2-picoline, pyridine and 4-picoline is added in the reaction flask through a constant pressure funnel and stirred evenly, wherein two The mass ratio of toluene to the pyridine base mixture is 3:1, 2-picoline accounts for 55% of the total mass, 28% of pyridine, and 17% of 4-picoline in the pyridine base mixture;

[0067] (b) Slowly heating the reaction flask in step (a) to 135° C. for reflux dehydration until no water droplets are produced in the reaction flask;

[0068] (c) After the dehydration reaction in step (b) is finished, it is cooled to room temperature, and sodium amide is added in the reaction flask with a speed of 20g / min and stirred evenly, and then micro-reflux reaction is carried out, wherein the mass of sodium amide and pyridine base mixture T...

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

PropertyMeasurementUnit
boiling pointaaaaaaaaaa
melting pointaaaaaaaaaa
Login to view more

Abstract

The invention discloses a method for synthesizing aminopyridine with a pyridine base mixture as well as a separation and purification method of the aminopyridine and belongs to the field of fine chemical engineering. According to the method, the pyridine base mixture reacts with sodium amide under proper conditions, then a mixture of 2-amino-4-methylpyridine, 2-aminopyridine and 2-amino-6-methylpyridine is obtained through a hydrolysis reaction, the 2-amino-4-methylpyridine, the 2-aminopyridine and the 2-amino-6-methylpyridine are separated one by one according to different melting points and different boiling points of all the components in the mixture, and the high-purity 2-amino-4-methylpyridine, the high-purity 2-aminopyridine and the high-purity 2-amino-6-methylpyridine are obtained. The synthesizing method and the separation and purification method have the advantages of simple technology, reasonable design, convenience in operation, and the synthesizing method is an environment-friendly synthesizing technology and has the broad application prospect.

Description

technical field [0001] The invention belongs to the field of fine chemical industry, in particular, relates to a method for synthesizing chemical intermediates, more specifically, relates to a method for synthesizing aminopyridine from a mixture of pyridine bases and a separation and purification method thereof. Background technique [0002] Pyridine compounds are currently one of the most widely developed and applied varieties of heterocyclic compounds. As an important fine chemical raw material, its derivatives mainly include alkylpyridine, halogenated pyridine, aminopyridine, bromopyridine, picoline , iodopyridine, chloropyridine, nitropyridine, hydroxypyridine, benzylpyridine, ethylpyridine, cyanopyridine, fluoropyridine, dihydropyridine, etc. Among them, pesticides account for about 50% of the total consumption of pyridine series products, feed additives About 30%, medicine and other fields accounted for 20%. Pyridine base compounds are important raw materials for orga...

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): C07D213/73
CPCC07D213/73
Inventor 张宽宇金文艺丁亮刘进水张升
Owner ANHUI XINGYU CHEM
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products