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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28109Generated: October 26, 2026

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

https://huagongshe.com/reaction/28109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
ReactantSodium HydroxideHCID 14798—
ReactantCyclopropylamineHCID 69828—
SolventChlorobenzeneHCID 7964—
Product4,6-Dichloro-N-cyclopropyl-1,3,5-triazin-2-amineHCID 22254066—

Reaction Conditions

Temperature-10 °C

Reaction Steps

133 g of cyanuric chloride are suspended in 720 ml of chlorobenzene and cooled to -10° C. To this suspension are added with stirring 50 ml of cyclopropylamine dropwise over a period of 25 minutes. Keeping the temperature at -10° C., 96 ml of aqueous sodium hydroxide (30% NaOH) are added dropwise. The reaction mixture is then stirred at -10° C. for 11/2 hours and allowed to stand for a further 16 hours at room temperature, after which it is washed with water (2×400 ml), dried over anhydrous sodium sulphate and filtered. The excess chlorobenzene is then removed by water jet vacuum distillation. 138 g of 2-cyclopropylamino-4,6-dichloro-s-triazine in the form of white crystals are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225598
Source datasetuspto-grants-1980_09
ORD IDord-8cad7758f10c4a5abd3dddc305038682
Source noteuspto-grants-1980_09