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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469908Generated: October 25, 2026

6-Bromo-3,5-dimethoxypicolinonitrile → 6-Ethyl-3,5-dimethoxy-pyridine-2-carbonitrile

https://huagongshe.com/reaction/1469908

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-3,5-dimethoxypicolinonitrileHCID 73554911—
ReactantHCID 178418443HCID 178418443—
CatalystDichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickelHCID 2724937—
SolventTetrahydrofuranHCID 8028—
Product6-Ethyl-3,5-dimethoxy-pyridine-2-carbonitrileHCID 66986777—

Reaction Conditions

Temperature0 °C

Reaction Steps

Impure 6-bromo-3,5-dimethoxy-pyridine-2-carbonitrile (462 mg; <1.9 mmol) was dissolved in tetrahydrofuran (20 mL) under nitrogen, and to the solution was added 1,3-bis(diphenylphosphino)propane nickel (II) chloride (105 mg; 0.19 mmol). The solution was cooled to 0° C., and a solution of ethyl magnesium bromide (1.0 molar in THF; 2.7 mL; 1.4 eq.) was slowly added. The reaction was stirred for five minutes, and quenched with saturated aqueous ammonium chloride (10 mL). To the reaction was added ethyl acetate (40 mL) and water (40 mL). The organic layer was isolated, dried over sodium sulfate, evaporated, and purified by column chromatography to give 6-ethyl-3,5-dimethoxy-pyridine-2-carbonitrile (114 mg; 0.6 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006277B2
Source datasetuspto-grants-2015_04
ORD IDord-5c04511f044a42518957de848fda3f4a
Source noteuspto-grants-2015_04