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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598947Generated: November 3, 2026

Hydrochloric Acid → 1,3,5-Triazin-2-amine, 4-ethoxy-6-(trifluoromethyl)-

https://huagongshe.com/reaction/1598947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl trifluoroacetateHCID 9794—
ReactantSodium ethoxideHCID 2723922—
ReactantCalcium ChlorideHCID 5284359—
ReactantHCID 178418324HCID 178418324—
SolventEthanolHCID 702—
Product1,3,5-Triazin-2-amine, 4-ethoxy-6-(trifluoromethyl)-HCID 19994789%

Reaction Steps

8.4 g (0.1 mol) of cyanoguanidine and 35.5 g (0.25 mol) of ethyl trifluoroacetate are initially introduced into 46 g of ethanol, and a suspension of 8.5 g (0.125 mol) of sodium ethoxide in 39.8 g of ethanol is added in the course of 5 min. After the addition of 5.66 g (0.05 mol) of calcium chloride, the reaction mixture is heated to reflux for 7 hours. 0.5 ml of a conc. hydrochloric acid is then added at 20° C. and the ethanol is removed. 100 g of water are added and the suspension is filtered with suction. The residue is washed with 50 ml of water and dried at 50° C./20 mbar. 18.6 g (0.089 mol, 89%) of 2-amino-4-ethoxy-6-trifluoromethyl-1,3,5-triazine are obtained in the form of a colorless powder (HPLC: 99.8 area %, m.p. 124°-125° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739328
Source datasetuspto-grants-1998_04
ORD IDord-332a7fc1d056469db36fcd54e4fb80fa
Source noteuspto-grants-1998_04