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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586219Generated: November 1, 2026

Sodium Hydroxide → 5-(Trifluoromethyl)-1,2,4-triazin-3-amine

https://huagongshe.com/reaction/586219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,1-Dibromo-3,3,3-trifluoroacetoneHCID 550523—
ReactantSodium Acetate TrihydrateHCID 23665404—
ReactantHCID 178513185HCID 178513185—
SolventWaterHCID 962—
Product5-(Trifluoromethyl)-1,2,4-triazin-3-amineHCID 1154283253.1%

Reaction Steps

To a stirred solution of sodium acetate trihydrate (22.62 g, 166.2 mmol) in water (80 ml) was added 1,1-dibromo-3,3,3-trifluoroacetone (21.57 g, 79.9 mmol). The solution was heated at reflux under nitrogen for 30 min, then allowed to cool to room temperature before adding solid aminoguanidine bicarbonate (10.88 g, 79.9 mmol). The resulting pale yellow solution (pH 5) was stirred at room temperature for 3 h, then 4 N aqueous NaOH solution (40 ml, 160 mmol) was added causing a precipitate to appear. The mixture (pH 10) was stirred under nitrogen for a further 39 h. The solid was collected by filtration, washed with water and dried at 60° C. under vacuum to give 6.96 g of a mixture of two isomers in a 28:72 ratio. This was further purified by flash chromatography (silica gel, 30% EtOAc/isohexane), then recrystallised from ethanol to afford 3.53 g (27%) of the title compound: 1H NMR (400 MHz, DMSO-d6) δ 8.00 (2H, br s), 9.08 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936608B2
Source datasetuspto-grants-2005_08
ORD IDord-f2147dba36774a0aa39f6c040f9baf9b
Source noteuspto-grants-2005_08