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

Process for synthesizing 1-amino-anthraquinone-2-sulfonic acid through solid-phase method

A technology of aminoanthraquinone and solid-phase method, which is applied to the preparation of sulfonic acid, chemical instruments and methods, and the preparation of organic compounds. To achieve the effect of low production cost

Inactive Publication Date: 2018-06-08
DALIAN HEPTACHROMA SOLAR TECH CO LTD
View PDF15 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The disadvantage is that there are many impurities generated and the yield is low. Even if the quality is repeatedly refined, it cannot reach the level of the chlorosulfonic acid method, and the amount of "three wastes" is large.

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
  • Process for synthesizing 1-amino-anthraquinone-2-sulfonic acid through solid-phase method
  • Process for synthesizing 1-amino-anthraquinone-2-sulfonic acid through solid-phase method
  • Process for synthesizing 1-amino-anthraquinone-2-sulfonic acid through solid-phase method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] In the solid phase reactor of 10L, add the ceramic ball that the diameter of 3kg is 10cm, add the content of 2.28kg then and be 98% 1-aminoanthraquinone (10mol) and the mass fraction of 1.2kg be 98% sulfuric acid (12mol ), the reactor was rotated for 3 hours to fully mix 1-aminoanthraquinone and sulfuric acid to form a salt, and the temperature was raised to 180°C. After reacting for 15 hours, the content of 1-aminoanthraquinone-2-sulfonic acid in the product was measured by liquid chromatography to be 97.3%, and the content of 1-aminoanthraquinone was 2.7% (area normalization method).

[0034] Attachment: Further synthesis of bromic acid:

[0035] Use 30L of water to wash the product in the solid-phase reactor several times, put it in a 200L bromination pot, add ice water to adjust the volume to 90L, the temperature to 0-5°C, adjust the pH value to 2, and add bromine dropwise at the same time element and NaClO aqueous solution, and keep the temperature at 0-5°C, adjus...

Embodiment 2

[0037] In a 20L reactor, add 10kg of dichloroethane, 2.28kg of 98% 1-aminoanthraquinone (10mol) and 1.01kg of 98% mass fraction of sulfuric acid (10.1mol), fully stir to make 1 -Aminoanthraquinone and sulfuric acid are fully mixed to form a salt. At the same time, the temperature is raised to distill dichloroethane, and then the temperature is raised to 200°C, and the vacuum is evacuated to an absolute vacuum of 10mmHg to take out the water vapor generated by the reaction. Keep the reaction for 8h. The content of 1-aminoanthraquinone-2-sulfonic acid in the product measured by liquid chromatography is 99.2%, and the content of 1-aminoanthraquinone is 0.8% (area normalization method).

[0038] Attachment: Further synthesis of bromic acid:

[0039] Using the same method as in Example 1, 3.95kg of bromic acid product was obtained, content (calculated as bromic acid sodium salt, MW404): 96.5%, liquid chromatography purity: 100%, from 1-aminoanthraquinone to bromic acid The overall...

Embodiment 3

[0041] In a 20L reactor, add 10kg of chlorobenzene, 2.28kg of 98% 1-aminoanthraquinone (10mol) and 1.05kg of 98% sulfuric acid (10.5mol) in mass fraction, fully stir to make 1-aminoanthraquinone Anthraquinone and sulfuric acid are fully mixed to form a salt. At the same time, the temperature is raised to distill chlorobenzene, and then the temperature is raised to 180°C, and the vacuum is evacuated to an absolute vacuum of 10mmHg to take out the water vapor generated by the reaction. Keep the reaction for 15h, and use liquid chromatography The measured content of 1-aminoanthraquinone-2-sulfonic acid in the product is 99.4%, and the content of 1-aminoanthraquinone is 0.6% (area normalization method).

[0042] Attachment: Further synthesis of bromic acid:

[0043]Add 6kg of 98% sulfuric acid to the above reaction kettle, heat up to 80°C, add 0.6kg of bromine dropwise in 8 hours under reflux, react at 80°C for 2h, cool down to room temperature, add 12kg of water dropwise, filter ...

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
Diameteraaaaaaaaaa
Login to View More

Abstract

The invention provides a method for synthesizing 1-amino-anthraquinone-2-sulfonic acid from 1-amino-anthraquinone. The method comprises the following steps: generating a sulfate solid of 1-amino-anthraquinone through reaction of the 1-amino-anthraquinone and sulfuric acid, and then performing transposition on the sulfate solid of the 1-amino-anthraquinone to generate the 1-amino-anthraquinone-2-sulfonic acid. A process of synthesizing the 1-amino-anthraquinone-2-sulfonic acid by a sulfuric acid method is fundamentally improved; the sulfate of the 1-amino-anthraquinone is efficiently subjectedto transposition reaction under a solid-phase condition without a solvent after generated water is removed, so that the reaction yield is high, and no side effects are caused; furthermore, no 1-amino-4-chloroant-2-sulfonic acid is generated, and no wastewater, waste gas and waste residues are generated; an obtained product is further synthesized into bromamine acid, and the purity of the obtainedbromamine acid is close to 100 percent; the quality and the yield of the bromamine acid are both higher than the quality and the yield of bromamine acid synthesized by a chlorosulfonic acid method, afuming sulfuric acid method and a conventional sulfuric acid method.

Description

technical field [0001] The invention relates to a synthesis process of an important dye intermediate 1-aminoanthraquinone-2-sulfonic acid. Background technique [0002] The main purpose of 1-aminoanthraquinone-2-sulfonic acid described in the present invention is further bromination synthesis 1-amino-4-bromoanthraquinone-2-sulfonic acid sodium salt (being commonly called as bromic acid), and bromic acid is A very important intermediate for synthetic dyes, used to synthesize many excellent reactive dyes, acid dyes, disperse dyes, etc. The structural formula of 1-aminoanthraquinone-2-sulfonic acid is as follows: [0003] [0004] 1-aminoanthraquinone-2-sulfonic acid is synthesized by sulfonating 1-aminoanthraquinone. The synthesis process can be divided into three types according to the sulfonating agent used. [0005] 1. Chlorosulfonic acid method: disperse 1-aminoanthraquinone in chlorobenzene, o-dichlorobenzene, and nitrobenzene inert organic solvents, form a salt with...

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): C07C309/53C07C303/02C07C225/30C07C221/00
CPCC07C221/00C07C303/02C07C225/30C07C309/53
Inventor 杨希川
Owner DALIAN HEPTACHROMA SOLAR TECH 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