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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2,4-DinitroanilineHCID 7321—
ReactantNitrosylsulfuric acidHCID 82157—
Reactant2,5-Bis(2-ethylhexyloxy)anilineHCID 89601757—
SolventAcetic AcidHCID 176—
SolventPropionic AcidHCID 1032—
SolventSulfamic AcidHCID 5987—
Product4-((2,4-Dinitrophenyl)diazenyl)-2,5-bis(2-ethylhexyloxy)anilineHCID 8960207439%

Reaction Conditions

Temperature3 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09383621B2
Source datasetuspto-grants-2016_07
ORD IDord-ad3dc1c3e5ec46369746086868cd0366
Source noteuspto-grants-2016_07