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

DSD acid preparation method

A technology of mixing acid and sulfuric acid, applied in the preparation of sulfonic acid, organic chemistry, etc., can solve the problems of low purity of finished products and high production labor intensity, and achieve the effects of high purity, short reaction time, and reduction of waste formation.

Active Publication Date: 2016-11-23
上海合丽亚日化技术有限公司
View PDF7 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This method is simple to operate, low in production cost, and easy to control, but it will produce a large amount of solid waste iron sludge
In addition, the production is labor-intensive, and the product often contains a certain amount of iron compounds, DADB and non-fluorescent cis-DAS, resulting in low purity of the finished product

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
  • DSD acid preparation method
  • DSD acid preparation method
  • DSD acid preparation method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0070] In the 500ml four-necked reaction flask, add 48.80g toluene, 0.30g catalytic fixer SO4 2- / ZrO 2 -TiO 2 , under electric stirring, the frozen brine is cooled to about -5~0°C, and the measured 98% concentrated sulfuric acid is slowly added dropwise, and the dropping time is controlled within 2~10 hours. until the reaction is complete. The reaction solution changed from cloudy to light yellow-green transparent liquid. Sample HPLC analysis, OTS 81.09%, PTS 17.65%. Add the reaction liquid to an appropriate amount of ice water, adjust the concentration of sulfuric acid to 75%, stir at a temperature of 10-15°C, keep stirring for 6 hours, and filter with suction to obtain a PTS filter cake (HPLC content 96.73%). The proton nuclear magnetic resonance spectrum of the prepared PTS is as follows figure 1 As shown, the carbon NMR spectrum is as figure 2 shown.

[0071] Carefully transfer the filtrate to another 500ml four-necked reaction bottle, adjust the acidity to 80%, c...

Embodiment 2

[0075] Add PNTS (100%) 56.7g synthesized in embodiment 1 in the 1L four-necked flask, 0.20g Cu-Fe-MnO x / TiO 2 , 600ml of water. A redox electrode and a potential measurement and control system are installed in the reaction bottle. Stir and heat up to 35°C, and slowly add 31.68% liquid caustic soda dropwise. When the temperature rises to 45°C, chlorine gas is introduced, and the reaction is exothermic. At this time, the temperature is gradually increased, and the flow rate and pressure of the chlorine gas are controlled so that the oxidation-reduction potential of the reaction system is between -100 and +100. As the reaction progressed, the reaction solution became turbid, and the color gradually changed from light yellow to light amber. After 1 hr, when the temperature rose to 75°C, the temperature was kept for 15 minutes, and the solution became clear, so the dropwise addition of liquid caustic soda was stopped. Liquid caustic soda consumes 170ml. HPLC analysis showed t...

Embodiment 3

[0077] In the 1L four-necked flask, add 56.7g of PNTS (100%) synthesized in Example 1, 0.20g Cu-Ce-MnO x / TiO 2， 500ml of water, redox electrode and potential measurement and control system are installed in the reaction bottle. Stir and heat up to 45° C., start to drop 170 ml of 31.68% liquid caustic soda, and feed chlorine gas when the pH value of the reaction solution is ≥10, and operate the potentiometric measurement and control system according to Example 2. When the temperature rose to 65°C, 150ml of water was added dropwise, and the addition was completed within half an hour. Finally, the temperature rose to 85°C and the solution became clear. HPLC analysis of PNTS content ≤ 1.0%, stop feeding chlorine, the reaction is over. Reaction time 105 minutes. Cooling crystallization and suction filtration, adding the waste acid produced in Example 2 dropwise to the mother liquor, adjusting the pH value to 3, and then suction filtration. The two filter cakes were evenly mixe...

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 relates to the field of chemical synthesis, in particular to a DSD acid preparation method. The DSD acid preparation method includes the steps that methylbenzene is subjected to sulfonation, purification and separation to obtain OTS, wherein the byproduct is PTS; OTS is subjected to mixed acid nitration to obtain PNTS; PNTS is subjected to chlorine oxidative condensation to obtain DNS; DNS is subjected to catalyzed hydrogeneration reduction to obtain the high-quality target product, namely DSD acid which can be directly used for synthesizing a fluorescent whitening agent. The synthesis method greatly reduces dangerousness of the process, greatly reduces generation of harmful byproducts and waste, particularly, does not generate a lot of carcinogenic intermediate, namely ortho-nitrotoluene, completely solves the nitration safety problem of the old technology, and has the advantages of being simple in step, high in yield and the like.

Description

technical field [0001] The invention relates to the field of chemical synthesis, in particular to a method for preparing DSD acid. Background technique [0002] The full name of DSD acid is 4,4'-diaminostilbene-2,2'-disulfonic acid, also referred to as D acid or DAS. It is an important intermediate for the synthesis of various fluorescent whitening agents, direct dyes, and reactive dyes, and can also be used to synthesize insecticides. The current synthesis process is as follows: p-nitrotoluene (PNT) is obtained by nitration and purification of toluene with mixed acid, and then sulfonated with fuming acid to obtain p-nitrotoluene orthosulfonic acid (PNTS). Two molecules of PNTS are oxidized under alkaline conditions. Condensation produces 4,4'-dinitrostilbene-2,2'-disulfonic acid (DNS), and then iron powder reduces DNS to obtain 4,4'-diaminostilbene-2,2'-di Sulfonic acid (DSD acid). The current above-mentioned process route has many potential safety hazards, produces a la...

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 Applications(China)
IPC IPC(8): C07C303/22C07C309/46C07C303/06C07C309/30
Inventor 张贵民孙桥
Owner 上海合丽亚日化技术有限公司
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

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