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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75939Erstellt: 23. Oktober 2026

Iodine → 2,6-Dichloro-5-fluoro-4-iodonicotinonitrile

https://huagongshe.com/de/reaction/75939

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktDiisopropylamineHCID 7912—
EduktSodium ThiosulfateHCID 24477—
EduktLithium diisopropylamideHCID 2724682—
Edukt2,6-Dichloro-5-fluoro-3-pyridinecarbonitrileHCID 2733849—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,6-Dichloro-5-fluoro-4-iodonicotinonitrileHCID 8662062387,5%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of diisopropylamine (15.9 g, 157 mmol) in THF (400 ml) at −78° C. was added n-butyllithium (2.5 M hexanes, 154 mmol), and the solution was stirred at −78° C. for 30 minutes. The lithium diisopropylamide solution was then added slowly dropwise to a −78° C. solution of 2,6-dichloro-5-fluoronicotinonitrile (10.0 g, 52.3 mmol) and iodine (26.5 g, 104 mmol) in THF (175 ml). Upon completion of the addition, the reaction was allowed to warm slowly to room temperature, and stirred at room temperature for 12 hours. An aqueous 10% Na2S2O3 solution (500 ml) was added and the reaction was extracted with EtOAc (3×300 ml). The combined organic fractions were dried over Na2SO4, filtered, and then concentrated to give the title compound (14.5 g, 87%) as a brown solid that was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835465B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-808231e5a3284e5489291033d5ce8883
Quellennotizuspto-grants-2014_09