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

Preparation method of 3-cyanopyridine oxynitride

A technology of cyanopyridine nitrogen oxide and cyanopyridine, which is applied in the field of preparation of chemical intermediates, can solve the problems of difficulty in improving enterprise benefits, high production costs, poor market competitiveness, etc., and achieves fast reaction speed and increased affinity. The effect of shortening electric capacity and reaction time

Inactive Publication Date: 2013-11-27
WUXUE YONGNING MEDICAL & CHEM CO LTD
View PDF4 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Because this method uses expensive sodium tungstate (160-180 yuan / kg) as a catalyst, the reaction temperature is high, the reaction time is long, and the yield is low. Therefore, the production cost has been high (48000- 50,000 yuan / kg), poor market competitiveness, difficult to improve corporate efficiency

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-cyanopyridine oxynitride

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0010] Example 1, take 500kg of barreled 3-cyanopyridine, put it into hot water at 70-80°C and slowly melt it, then add it to the enamel reaction kettle, then add 10kg of concentrated sulfuric acid and 8kg of molybdenum oxide into the reaction kettle, and stir , slowly raise the temperature to 65°C, start to add hydrogen peroxide dropwise, and control the dropping rate to 200kg / h. When the pyridine content is ≤1.0%, stop the heat preservation; adjust the reaction liquid with potassium carbonate to pH 9.5-10.5, crystallize, cool down to below 5°C, centrifuge, take the crystal and dry it at 80-90°C to obtain 3-cyano Pyridine nitrogen oxide; after testing, content: ≥98.0%, moisture: ≤1.0%, 3-cyanopyridine: ≤1.0%, meeting the quality requirements.

[0011] The technical and economic indicators of the 3-cyanopyridine nitrogen oxides prepared by embodiment 1 and the prior art are shown in the table below:

[0012]

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 discloses a preparation method of 3-cyanopyridine oxynitride. The preparation method is characterized by comprising the following steps of: melting 500kg of 3-cyanopyridine, adding the molten 3-cyanopyridine into an enamel reaction kettle, adding 10kg of concentrated sulfuric acid and 8kg of molybdenum oxide into the reaction kettle, stirring the mixture, slowly heating to 65 DEG C, beginning to dropwise add hydrogen peroxide, controlling the dropping speed at about 200kg / h, after the dropwise adding operation is ended, continuing to react at the temperature of 65-68 DEG C for 7-8h, sampling, detecting the sample by using gas chromatography, and ending the heat preservation when the content of the 3-cyanopyridine is lower than or equal to 1.0%; and adjusting the pH value of the reaction liquid to 9.5-10.5 by using potassium carbonate, crystallizing, cooling the crystal to be below 5 DEG C, centrifuging, and drying the crystal at the temperature of 80-90 DEG C to obtain the 3-cyanopyridine oxynitride, wherein the water content of the 3-cyanopyridine oxynitride is smaller than or equal to 1.0%. Compared with the prior art, the preparation method has the advantage that the production cost is greatly reduced, so that the economic benefit and market competitiveness of an enterprise are increased.

Description

technical field [0001] The invention relates to a preparation method of a chemical intermediate, in particular to a preparation method of 3-cyanopyridine nitrogen oxide. Background technique [0002] 3-cyanopyridine nitrogen oxide is the main intermediate for the production of nicotinic acid and nicotinamide, and its production cost determines the final cost of nicotinic acid and nicotinamide, which in turn determines the economic benefits of the enterprise. The preparation method disclosed in the current literature is to oxidize 3-cyanopyridine with hydrogen peroxide under the action of sulfuric acid and catalyst sodium tungstate, the molar ratio of hydrogen peroxide to 3-cyanopyridine is 1:4, and the reaction temperature is 90°. The reaction time was 20 hours, and the yield was only 94% (based on 3-cyanopyridine). Because this method uses expensive sodium tungstate (160-180 yuan / kg) as a catalyst, the reaction temperature is high, the reaction time is long, and the yield ...

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
IPC IPC(8): C07D213/89
Inventor 张群刘亚金
Owner WUXUE YONGNING MEDICAL & CHEM CO LTD
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com