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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2407Erstellt: 24. Oktober 2026

Water → N-(2-Methoxyphenyl)-4-methylbenzenesulfonamide

https://huagongshe.com/de/reaction/2407

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPyridineHCID 1049—
Edukt2-MethoxyanilineHCID 7000—
Edukt4-Toluenesulfonyl chlorideHCID 7397—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelTolueneHCID 1140—
ProduktN-(2-Methoxyphenyl)-4-methylbenzenesulfonamideHCID 24173162%

Reaktionsschritte

o-Anisidine (2.34 ml, 20 mmol) was dissolved in toluene (60 ml) to which were subsequently added, with cooling in an ice bath, pyridine (4.58 ml, 60 mmol), p-toluenesulfonyl chloride (3.89 g, 20 mmol) and a catalytically effective amount of 4-dimethylaminopyridine. After 2.5 hours of stirring at room temperature, the resulting reaction solution was mixed-with water (50 ml), extracted with ethyl acetate and then washed with water, 10% sodium hydroxide aqueous solution, 1N hydrochloric acid, water and saturated brine in that order. After drying on anhydrous magnesium sulfate and removing the solvent by evaporation, the resulting orange solid was dissolved in ethyl acetate (50 ml), adsorbed to anhydrous magnesium sulfate (20 g), eluted with ether and then subjected to evaporation to remove the solvent. The resulting colorless solid which was then washed with an ether-hexane (1:1) mixture solution to obtain 3.44 g (62.0%) of the title compound in the form of colorless prism crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728835
Quelldatensatzuspto-grants-1998_03
ORD IDord-04e2e891f8e24233803e97b3a1a02cf4
Quellennotizuspto-grants-1998_03