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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392369Generated: October 29, 2026

Water → 6-Fluoro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile

https://huagongshe.com/reaction/392369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium FluorideHCID 522689—
Reactant6-Chloro-3-(phenylsulfanyl)-2-pyrazinecarbonitrileHCID 22662804—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDimethyl SulfoxideHCID 679—
Product6-Fluoro-3-(phenylsulfanyl)-2-pyrazinecarbonitrileHCID 2266284953.6%

Reaction Conditions

Temperature55 °C

Reaction Steps

In 3.6 mL of dimethyl sulfoxide was dissolved 0.20 g of 6-chloro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile. After adding 0.42 g of potassium fluoride and 0.16 g of tetra-n-butylammonium bromide successively, the mixture thus obtained was stirred at 50-60° C. for 2.5 hours. The reaction mixture was poured into a mixture of 20 mL of ethyl acetate and 20 mL of water, and the organic layer was separated. The organic layer was washed successively with water and 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: toluene:n-hexane=1:2] to obtain 0.10 g of 6-fluoro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile as a light yellow-colored oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800629B2
Source datasetuspto-grants-2004_10
ORD IDord-4c2f1268c881457ba9eac2091be0501b
Source noteuspto-grants-2004_10