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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 56719Erstellt: 24. Oktober 2026

Iodine → 4-Iodo-6-methoxynicotinonitrile

https://huagongshe.com/de/reaction/56719

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktAmmonium ChlorideHCID 25517—
EduktLithium diisopropylamideHCID 2724682—
Edukt2-Methoxy-5-pyridinecarbonitrileHCID 2736776—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Iodo-6-methoxynicotinonitrileHCID 117605412—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

At −78° C., 19.4 ml of lithium diisopropylamide (2 molar in THF/heptane/ethylbenzene, 1.3 eq.) were added to a solution of 4.0 g (29.8 mmol) of 6-methoxypyridine-3-carbonitrile in 120 ml of THF, and the mixture was stirred at −78° C. for 1 h. At −78° C., a solution of 9.1 g (35.8 mmol) of iodine in 20 ml of THF was then added, and the reaction mixture was stirred at −78° C. for 1 h and then carefully added to saturated aqueous ammonium chloride solution. After addition of ethyl acetate, the reaction mixture was extracted three times with ethyl acetate. The combined organic phases were dried (magnesium sulphate), filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography (silica gel 60, mobile phase: cyclohexane/ethyl acetate mixtures). Yield: 4.0 g (purity 92%, 48% of theory)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434690B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-7152e453c2da495a95d1b2cf28d7baa1
Quellennotizuspto-grants-2016_09