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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598945Generated: October 27, 2026

Methyl trifluoroacetate → 4-Methoxy-6-(trifluoromethyl)-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1598945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl trifluoroacetateHCID 9893—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178418324HCID 178418324—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
Product4-Methoxy-6-(trifluoromethyl)-1,3,5-triazin-2-amineHCID 19994889%

Reaction Conditions

Temperature50 °C

Reaction Steps

21 g (0.25 mol) of N-cyanoguanidine, 3.4 g (0.025 mol) of anhydrous zinc chloride and 160 g (1.25 mol) of methyl trifluoroacetate are initially introduced into 400 ml of methanol, the mixture is warmed to 50° C. and 50 g (0.27 mol) of 30% strength sodium methoxide solution are pumped in in the course of 10 hours. The solvent is then largely removed, and the residue is washed with 250 ml of water and 250 ml of dilute hydrochloric acid and dried at 60° C./20 mbar. 43.2 g (0.22 mol, 89%) of 2-amino-4-trifluoromethyl-6-methoxy-1,3,5-triazine are obtained in the form of a colorless powder (HPLC: >99% by weight) M.p.: 161°-163.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739328
Source datasetuspto-grants-1998_04
ORD IDord-dcaf4672fd02481fbfdf148f3c173295
Source noteuspto-grants-1998_04