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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376697Generated: October 31, 2026

Urea → 3-Methyl-4-((4-nitrophenyl)azo)benzenamine

https://huagongshe.com/reaction/1376697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
Reactant4-NitroanilineHCID 7475—
Reactantm-ToluidineHCID 7934—
ReactantPotassium CarbonateHCID 11430—
Reactantm-Toluidine hydrochlorideHCID 522105—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product3-Methyl-4-((4-nitrophenyl)azo)benzenamineHCID 43991195%

Reaction Steps

Recrystallized 4-nitroaniline (16.5 g, 0.12 mol) was dissolved in 10N hydrochloric acid (40 ml) at 75° C. The solution was diluted with water (40 ml), poured over ice (100 g), and cooled in an ice bath. Sodium nitrite solution (64.0 ml, 2M) was added over 5 minutes and the mixture was stirred for 30 minutes. Urea (1.0 g) was added and the mixture was stirred 20 minutes in an ice bath. In a separate beaker distilled m-toluidine (17.1 g, 0.16 mol) was mixed with 5N hydrochloric acid (40 ml) for 5 minutes at room temperature and then cooled in an ice bath. The diazonium salt solution was added all at once to the m-toluidine hydrochloride suspension. The mixture was stirred occasionally over 2 hours at 0°-5° C. The mixture was basified with saturated potassium carbonate and the resulting solid was washed twice with warm water. Recrystallization of the solid twice from tetrahydrofuran (90 ml) and ethanol (200 ml) gave 4-(4-nitrophenylazo)-3-methylaniline as red needles (8.32 g, 28%): mp 152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663308
Source datasetuspto-grants-1997_09
ORD IDord-13e3c84a6b0044219a1bbbe35e05331e
Source noteuspto-grants-1997_09