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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821626Generated: November 2, 2026

Aniline → HCID 791000, compound

https://huagongshe.com/reaction/1821626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4,6-dichloro-N-(4-chlorophenyl)-1,3,5-triazin-2-amineHCID 16763—
Catalyst18-Crown-6HCID 28557—
SolventTolueneHCID 1140—
ProductHCID 791000HCID 79100046%

Reaction Steps

To a mixture of (4-chloro-phenyl)-(4,6-dichloro-[1,3,5]triazin-2-yl)-amine (3.97 g, 14.4 mmol), potassium carbonate (2.20 g, 15.9 mmol) and 18-crown-6 (46 mg, 0.17 mmol) in toluene (25 ml), cooled in an ice bath, was added a solution of aniline (1.4 ml, 15.4 mmol) in toluene (10 ml) over 15 minutes. After stirring at room temperature for 24 hours, the mixture was treated with ethyl acetate (35 ml) and filtered through a pad of celite under suction. The filtrate was concentrated under vacuum and the residue was recrystallized (chloroform) to give 6-Chloro-N-(4-chlorophenyl)-N′-phenyl-[1,3,5]triazine-2,4-diamine (2.20 g, 46% yield) as a white solid. 1H NMR (d6-DMSO) δ 10.1-10.4 (2H, br s), 7.5-7.8 (4H, br s), 7.3-7.5 (4H, m), 7.15-7.05 (1H, m), ESMS m/z 330 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608620B2
Source datasetuspto-grants-2009_10
ORD IDord-24fccaf140424fcb8f8954cb1ab6e9c2
Source noteuspto-grants-2009_10