HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050494Generated: October 26, 2026
Sulfuric Acid → 4-((2,4-Dinitrophenyl)diazenyl)-2,5-bis(2-ethylhexyloxy)aniline
https://huagongshe.com/reaction/1050494
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,4-Dinitroaniline | HCID 7321 | — |
| Reactant | Nitrosylsulfuric acid | HCID 82157 | — |
| Reactant | 2,5-Bis(2-ethylhexyloxy)aniline | HCID 89601757 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Propionic Acid | HCID 1032 | — |
| Solvent | Sulfamic Acid | HCID 5987 | — |
| Product | 4-((2,4-Dinitrophenyl)diazenyl)-2,5-bis(2-ethylhexyloxy)aniline | HCID 89602074 | 39% |
Reaction Steps
2,4-Dinitroaniline (3.7 g, 0.02 mol) is suspended in a mixture of acetic acid (20 ml) and propionic acid (10 ml) and cooled to 3° C. 40% (w/w) nitrosyl sulfuric acid in sulfuric acid (6.4 g, 0.02 mol) is added dropwise and stirring continued for 30 minutes to give a pale yellow solution. Crude 2,5-bis(2-ethylhexyloxy)aniline (0.02 mol) solution is diluted with IMS (200 ml) and 10% sulfamic acid solution (20 ml) added, followed by ice (200 g). The above pale yellow diazonium salt solution is slowly added with stirring and a dark oil rapidly separated. The mixture is stirred overnight and the water is decanted off. The crude product (8.3 g) is dissolved in 25/75 dichloromethane/hexane and purified over silica gel, the required product eluting with 50/50 hexane/dichloromethane. Evaporation and trituration with methanol gave 4-((2,4-dinitrophenyl)diazenyl)-2,5-bis(2-ethylhexyloxy)-aniline as a violet-blue crystalline solid (4.2 g, 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09383621B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-ad3dc1c3e5ec46369746086868cd0366 |
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| Source note | uspto-grants-2016_07 |
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