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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1015816Erstellt: 27. Oktober 2026

3-Cyanobenzene-1-sulfonyl chloride → 3-(Aminomethyl)-N,N-dimethylbenzenesulfonamide

https://huagongshe.com/reaction/1015816

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Cyanobenzene-1-sulfonyl chlorideHCID 2801360—
EduktDimethylamine methanolHCID 22497844—
Produkt3-(Aminomethyl)-N,N-dimethylbenzenesulfonamideHCID 16795356—

Reaktionsschritte

(Step 1) To a 2M dimethylamine methanol solution (3.7 ml) was added 3-cyanobenzenesulfonyl chloride (1.5 g) at 0° C., and the mixture was stirred at room temperature for 2 hr. The solvent was evaporated under reduced pressure, saturated brine was added, and the mixture was extracted with ethyl acetate. The solvent was evaporated under reduced pressure. 10% Palladium carbon powder (0.79 g) was added to a solution (10 ml) of the residue in ethanol, and the mixture was stirred overnight under a hydrogen atmosphere (1 atm). The solution was filtered through celite. The solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate) to give 3-(aminomethyl)-N,N-dimethylbenzenesulfonamide (1.0 g) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07985863B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-5ffe55a3bb7b442aa465378dcbc9cecf
Quellennotizuspto-grants-2011_07