Clean synthesis of disperse azo dyes based on peculiar stable 2,6-dibromo-4-nitrophenyl diazonium sulfate
Source abstract
Abstract
Abstract The development of clean synthetic technology of disperse azo dyes is essential for the dye industry due to ecological and economical demands. In this study, a clean, safe, and low-energy-consumption method for preparing disperse azo dyes based on 2,6-dibromo-4-nitroaniline is presented with excellent yield and short reaction time. The peculiar stable diazonium sulfate of 2,6-dibromo-4-nitroaniline is precipitated from the organic reaction system, and the solid diazonium salt is directly used to synthesize disperse azo dyes. Compared with traditional method, the amount of sulfuric acid used is reduced by 80%, the amount of waste inorganic salt is reduced by 80.9% and the heat released from the reaction system is reduced by 88.5% in the proposed method. The dye structures are verified by 1H NMR, 13C NMR, Fourier transform infrared spectroscopy (FT-IR), and high resolution mass spectrometry (HR-MS). Compared with commercial dyes, the prepared dyes have the same dyeing properties that are sufficient for industrial applications.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Innovative Microfluidic and Catalytic Techniques Innovation · Dyeing and Modifying Textile Fibers · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (24)
Show source-provided references
1. Origins, current status, and future challenges of green chemistry10.1021/ar010065m ↗
2. Cleaner production of rubber seed oil methyl ester using a hydrodynamic cavitation: optimisation and parametric study10.1016/j.jclepro.2016.04.091 ↗
3. Cleaner Production in the textile industry and its relationship to sustainable development goals10.1016/j.jclepro.2019.04.334 ↗
4. Greener approaches to organic synthesis using microreactor technology10.1021/cr050944c ↗
5. Green chemistry: principles and practice10.1039/B918763B ↗
6. Clean and efficient synthesis of azo dyes using polymer-supported reagents10.1039/b000816h ↗
7. Convenient and rapid diazotization and diazo coupling reaction via aryl diazonium nanomagnetic sulfate under solvent-free conditions at room temperature10.1016/j.dyepig.2015.03.041 ↗
8. Rapid and efficient diazotization and diazo coupling reactions on silica sulfuric acid under solvent-free conditions10.1016/j.dyepig.2008.10.011 ↗
9. Nano-CuFe2O4-supported sulfonic acid as a novel and recyclable nanomagnetic acid for diazotization of aromatic amines: efficient synthesis of various azo dyes10.1007/s13738-016-0818-x ↗
10. Ionic liquid 1-(3-Trimethoxysilylpropyl)-3-methylimidazolium nitrite as a new reagent for the efficient diazotization of aniline derivatives and in situ synthesis of azo dyes10.1007/BF03249083 ↗
11. A new nitrite ionic liquid (IL-ONO) as a nitrosonium source for the efficient diazotization of aniline derivatives and in-situ synthesis of azo dyes10.1016/j.dyepig.2010.11.010 ↗
12. Nanoparticles of organosilane-based nitrite ionic liquid immobilized on silica for the diazotization of aniline derivatives and subsequent synthesis of azo dyes10.1016/j.dyepig.2011.09.013 ↗
13. Modified clays as efficient acid–base catalyst systems for diazotization and diazocoupling reactions10.1081/SCC-120016343 ↗
14. Application of modified clays in diazotization and azo coupling reactions in water10.1016/j.jiec.2011.11.146 ↗
15. A facile optimization of diazotization and phase transfer catalyzed azo-coupling reactions in microreactors10.1556/1846.2016.00003 ↗
16. The in situ generation and reactive quench of diazonium compounds in the synthesis of azo compounds in microreactors10.3762/bjoc.12.186 ↗
17. Study on the scale-up of phase-transfer-catalyzed azo coupling reactions in flow reactors10.1007/s10593-017-1990-3 ↗
18. Fast and high conversion phase-transfer synthesis exploiting the liquid-liquid interface formed in a microchannel chip10.1039/b106494k ↗
19. Dyeing with disperse dyes
20. Stable diazonium salts of weakly basic amines—convenient reagents for synthesis of disperse azo dyes10.1016/j.dyepig.2016.08.026 ↗
21. Facile synthesis of novel disperse azo dyes with aromatic hydroxyl group10.1016/j.dyepig.2018.08.052 ↗
22. Reactive chemical hazards of diazonium salts10.1016/j.jlp.2015.09.004 ↗
23. Ecofriendly synthesis and application of special disperse reactive dyes in waterless coloration of wool with supercritical carbon dioxide10.1016/j.jclepro.2016.05.187 ↗
24. A process-level water conservation and pollution control performance evaluation tool of cleaner production technology in textile industry10.1016/j.jclepro.2016.12.006 ↗