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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392332Generated: October 29, 2026

Ethyl Acetate → 6-Chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrile

https://huagongshe.com/reaction/392332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-MethoxyphenolHCID 9015—
ReactantPotassium CarbonateHCID 11430—
Reactant3,6-Dichloropyrazine-2-carbonitrileHCID 22662845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-Chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrileHCID 2266284893.1%

Reaction Steps

In 15 ml of dimethylformamide was dissolved 1.5 g of 3,6-dichloro-2-pyrazinecarbonitrile. After adding 1.2 g of 4-methoxyphenol and 1.8 g of potassium carbonate, the mixture thus obtained was stirred at room temperature for 30 minutes. A mixture of 20 mL of ethyl acetate and 60 mL of water was added to the reaction mixture, 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: n-hexane:ethyl acetate=5:1] to obtain 2.1 g of 6-chloro-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-7a00c41b2fdd4786ab99c6fb249a06bf
Source noteuspto-grants-2004_10