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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089682Generated: October 30, 2026

5-(Trifluoromethyl)pyrazin-2-amine → 5-(Trifluoromethyl)pyrazin-2-ol

https://huagongshe.com/reaction/1089682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Trifluoromethyl)pyrazin-2-amineHCID 13341115—
ReactantSodium NitriteHCID 23668193—
SolventSulfuric AcidHCID 1118—
Product5-(Trifluoromethyl)pyrazin-2-olHCID 19915808—

Reaction Steps

Sodium nitrite (0.21 g) was added in one batch to concentrated sulphuric acid (2.5 ml) at 2° C. The reaction mixture was then stirred, allowed to warm to room temperature and then heated to 40° C. for 10 minutes. The resulting solution was then cooled to 3° C. and a solution of 2-amino-5-trifluoromethylpyrazine (prepared by the method of Miesel, U.S. Pat. No. 4,293,552, 0.5 g) in concentrated sulphuric acid (3.5 ml) added dropwise. The reaction temperature was not allowed to rise above 5° C. during the addition. After stirring at 5° C. for 10 minutes, the reaction mixture was allowed to warm to room temperature and after 10 minutes heated to 40° C. for 10 minutes. The reaction mixture was then added to ice. Vigorous gas evolution was noted. The mixture was then extracted with ethyl acetate, the organic phase washed with brine, dried with sodium sulphate and evaporated under reduced pressure to give 5-trifluoromethylpyrazine-2-one as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079251
Source datasetuspto-grants-1992_01
ORD IDord-4c7128b5a9924892a72ead4d4b16c8f7
Source noteuspto-grants-1992_01