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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070441Generated: October 25, 2026

Cyanuric chloride → 4,6-Dichloro-N,N-dihexyl-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1070441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
ReactantDihexylamineHCID 8920—
ReactantSodium CarbonateHCID 10340—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4,6-Dichloro-N,N-dihexyl-1,3,5-triazin-2-amineHCID 10520613—

Reaction Steps

Dihexylamine (6.3 mL, 27 mmol) was added to a mixture of cyanuric chloride (5 0 g, 27 mmol) and sodium carbonate (2.9 g, 27 mmol) in acetonitrile (50 mL). The reaction mixture was heated to reflux for 16 h and then allowed to col to ambient temperature. The mixture was diluted with ethyl acetate and water. The phases were separated and the organic phase was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The crude material was purified by flash column chromatography through silica get (elution with 3:1 hexanes:chloroform) to afford 2,4-dichloro-6-dihexylamino-1,3,5-triazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903088B2
Source datasetuspto-grants-2005_06
ORD IDord-a4686081c0ed40b28d39d2922f8d2af7
Source noteuspto-grants-2005_06