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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1734621Erstellt: 24. Oktober 2026

Water → 2-Nitro-5-(4-chlorophenoxy)benzonitrile

https://huagongshe.com/de/reaction/1734621

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-ChlorophenolHCID 4684—
EduktSodium HydroxideHCID 14798—
Edukt5-Chloro-2-nitrobenzonitrileHCID 100506—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Nitro-5-(4-chlorophenoxy)benzonitrileHCID 2182487452,6%

Reaktionsschritte

Sodium hydride (60% in mineral oil), 1.5 grams (0.038 mole) was washed in petroleum ether. The petroleum ether was decanted, and the sodium hydride was suspended in about 20 mL of N,N-dimethylformamide. The suspension was stirred, and solutions of 4.5 grams (0.035 mole) of 4-chlorophenol in 20 mL of N,N-dimethylformamide and 5.0 grams (0.027 mole) of 5-chloro-2-nitrobenzonitrile in 20 mL of N,N-dimethylformamide were added, respectively. Upon completion of addition, the reaction mixture was warmed to reflux where it stirred for about 18 hours. The reaction mixture was then cooled and poured into a mixture of 500 mL of water and 50 mL of aqueous 2N sodium hydroxide. The mixture was stirred for about 15 minutes, then it was allowed to stand for about 18 hours. The resultant solid was collected by filtration and recrystallized from ethanol, yielding 3.9 grams of 2-nitro-5-(4-chlorophenoxy)benzonitrile, mp 120°-122° C. The NMR spectrum was consistent with the proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05534518
Quelldatensatzuspto-grants-1996_07
ORD IDord-bf5fb274188a445ba43d2a3cdbf96a9a
Quellennotizuspto-grants-1996_07