Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392366Generated: October 30, 2026

Water → 3-[4-(Benzyloxy)phenoxy]-6-fluoro-2-pyrazinecarbonitrile

https://huagongshe.com/reaction/392366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium FluorideHCID 522689—
Reactant3-[4-(Benzyloxy)phenoxy]-6-chloro-2-pyrazinecarbonitrileHCID 22662788—
SolventDimethyl SulfoxideHCID 679—
Product3-[4-(Benzyloxy)phenoxy]-6-fluoro-2-pyrazinecarbonitrileHCID 2266283456.5%

Reaction Conditions

Temperature105 °C

Reaction Steps

In 70 ml of dimethyl sulfoxide was dissolved 3.50 g of 3-[4-(benzyloxy)phenoxy]-6-chloro-2-pyrazinecarbonitrile. After adding 3.01 g of potassium fluoride, the mixture was stirred at 100-110° C. for 3 hours. The reaction mixture was returned to room temperature and added to a mixture of 70 mL of ethyl acetate and 350 mL of water, 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: toluene:ethyl acetate=5:1] to obtain 1.88 g of 3-[4-(benzyloxy)phenoxy]-6-fluoro-2-pyrazinecarbonitrile as a white-colored solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800629B2
Source datasetuspto-grants-2004_10
ORD IDord-dce0e30d812d4c8691137c57ac1a8d50
Source noteuspto-grants-2004_10