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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392365Generated: October 29, 2026

Water → 6-Fluoro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrile

https://huagongshe.com/reaction/392365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium FluorideHCID 522689—
Reactant6-Chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrileHCID 22662848—
SolventDimethyl SulfoxideHCID 679—
Product6-Fluoro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrileHCID 2266279179.3%

Reaction Conditions

Temperature105 °C

Reaction Steps

In 39 mL of dimethyl sulfoxide was dissolved 1.95 g of 6-chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrile. After adding 2.16 g of potassium fluoride, the mixture thus obtained was stirred at 100-110° C. for 3 hours. The reaction mixture was returned to room temperature, a mixture of 40 mL of ethyl acetate and 200 mL of water was added, and the organic layer was separated. The organic layer thus obtained was washed with saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent: n-hexane:ethyl acetate=5:1] to obtain 1.45 g of 6-fluoro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrile as a yellow-colored solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800629B2
Source datasetuspto-grants-2004_10
ORD IDord-3ec523f84f4545a9b2d2b207876a96c9
Source noteuspto-grants-2004_10