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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392334Generated: October 29, 2026

Methyl iodide → 6-Chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrile

https://huagongshe.com/reaction/392334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-3-(4-hydroxyphenoxy)-2-pyrazinecarbonitrileHCID 22662769—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-Chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrileHCID 22662848101.7%

Reaction Steps

In 8 mL of dimethylformamide was dissolved 0.4 g of 6-chloro-3-(4-hydroxyphenoxy)-2-pyrazinecarbonitrile. After adding 0.5 ml of iodomethane and 0.89 g of potassium carbonate, the mixture thus obtained was stirred at room temperature for 30 minutes. The reaction mixture was added to a mixture of 10 mL of ethyl acetate and 30 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. Thus, 0.43 g of 6-chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrile was obtained as a yellow-brown colored solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800629B2
Source datasetuspto-grants-2004_10
ORD IDord-d77dcb9fa0ed4b6d8870503764a58ad8
Source noteuspto-grants-2004_10