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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757606Generated: October 26, 2026

Cyanuric chloride → 4,6-dichloro-2-ethoxycarbonylmethylamino-S-triazine

https://huagongshe.com/reaction/1757606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
ReactantSodium BicarbonateHCID 516892—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Product4,6-dichloro-2-ethoxycarbonylmethylamino-S-triazineHCID 14746261—

Reaction Steps

36.9 g of cyanuric chloride, 27.9 g of ethyl glycinate hydrochloride and 33.6 g of sodium bicarbonate were heated under reflux in 200 ml of dioxanefor 30 minutes. At the end of this time, the dioxane was removed by distillation under reduced pressure, and a mixture of ethyl acetate and water was added to the resulting residue, after which the mixture was shaken. The ethyl acetate layer was separated, dried and concentrated by evaporation under reduced pressure, and the resulting residue was recrystallized from a mixture of hexane and ethyl acetate, to yield 45.0 gof the title compound as crystals melting at 82° to 87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446144
Source datasetuspto-grants-1995_08
ORD IDord-a263c55c9326424cab865273cb512687
Source noteuspto-grants-1995_08