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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971634Generated: October 30, 2026

Sodium Hydroxide → 6-(Trifluoromethyl)pyrazin-2-amine

https://huagongshe.com/reaction/971634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
Reactant1,1-Dibromo-3,3,3-trifluoroacetoneHCID 550523—
ReactantAminoacetamidine DihydrobromideHCID 16211382—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6-(Trifluoromethyl)pyrazin-2-amineHCID 13341114—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 6.6 g. of 3,3-dibromo-1,1,1-trifluoropropanone, 60 ml. of water, and 6.6 g. sodium acetate was refluxed for about 10 minutes. The solution thus obtained was cooled and added dropwise to a solution of 6 g. of aminoacetamidine dihydrobromide in 90 ml. of methanol cooled to a temperature of about -30° C., followed by the addition of a solution of 3.6 g. of sodium hydroxide pellets in 25 ml. of water. The reaction mixture was stirred and warmed gradually to about 20° C. over a period of about two hours. The reaction product mixture was concentrated in vacuo to remove the methanol, and the residue extracted with ethyl acetate. There was obtained product weighing 3.6 g. and having a melting point of about 133°-136° C. after recrystallization from a mixture of benzene and hexane. The product was identified by NMR spectrum and elemental analyses as 2-amino-6-trifluoromethylpyrazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160834
Source datasetuspto-grants-1979_07
ORD IDord-e995d15a1fc54fd9be66fa8282ce82c1
Source noteuspto-grants-1979_07