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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76097Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/76097

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Bromo-3,5-dimethoxypicolinonitrileHCID 73554911—
EduktHCID 178418443HCID 178418443—
KatalysatorDichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickelHCID 2724937—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-Ethyl-3,5-dimethoxy-pyridine-2-carbonitrileHCID 66986777—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835464B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-532f1d6b6fa349359073f09aec098b3b
Quellennotizuspto-grants-2014_09