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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1356704Erstellt: 26. Oktober 2026

Water → 4'-Chloro-4-cyano-N-ethyl-2'-nitrobenzenesulfonanilide

https://huagongshe.com/reaction/1356704

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt4-Cyanobenzenesulfonyl chlorideHCID 39497—
EduktBenzenamine, 4-chloro-N-ethyl-2-nitro-HCID 97006—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4'-Chloro-4-cyano-N-ethyl-2'-nitrobenzenesulfonanilideHCID 1850926564,6%

Reaktionsschritte

To a suspension of sodium hydride (60%, 0.10 g (2.50 mmol)) in tetrahydrofuran (THF)(3.0 ml), 4-chloro-N-ethyl-2-nitroaniline (0.40 g (1.99 mmol)) was added with stirring at room temperature. To the mixture, after stirring for 30 minutes at room temperature, 4-cyanobenzenesulfonyl chloride (0.50 g (2.48 mmol)) was added and the resulting mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into water and the resulting mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography with ethyl acetate-hexane (1:2) as eluent, to give 0.47 g (64%) of the title compound as pale yellow crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06586617B1
Quelldatensatzuspto-grants-2003_07
ORD IDord-ee92ba0fa7e3409690faf65a571f39f1
Quellennotizuspto-grants-2003_07