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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889071Generated: October 25, 2026

Water → 1-{[2-Chloro-3-(trifluoromethyl)phenyl]carbonyl}-5-(ethyloxy)-1,2,3,6-tetrahydropyrazine

https://huagongshe.com/reaction/1889071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactant4-{[2-Chloro-3-(trifluoromethyl)phenyl]carbonyl}-2-piperazinoneHCID 66599208—
SolventDichloromethaneHCID 6344—
Product1-{[2-Chloro-3-(trifluoromethyl)phenyl]carbonyl}-5-(ethyloxy)-1,2,3,6-tetrahydropyrazineHCID 66599399—

Reaction Steps

To a solution of 4-{[2-chloro-3-(trifluoromethyl)phenyl]carbonyl}-2-piperazinone (0.613 g, 2 mmol, e.g. as prepared in Intermediate 1) in Dichloromethane (5 ml) at room temperature was added triethyloxonium tetrafluoroborate (950 mg, 5.00 mmol). The reaction mixture was stirred for 18 hours. Dichloromethane (20 ml) and iced water (10 ml) were added and the pH was adjusted to pH 7 with solid sodium hydrogen carbonate. The organic phase was separated, washed with brine, dried and evaporated to give crude 1-{[2-chloro-3-(trifluoromethyl)phenyl]carbonyl}-5-(ethyloxy)-1,2,3,6-tetrahydropyrazine which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501946B2
Source datasetuspto-grants-2013_08
ORD IDord-19ef128f5b6843d9bd13a0f159348b45
Source noteuspto-grants-2013_08