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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 536047Erstellt: 24. Oktober 2026

Ammonium Chloride → HCID 24270770, Verbindung

https://huagongshe.com/de/reaction/536047

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktBenzenesulfonamide, 4-chloro-N-methyl-3-nitro-HCID 67301—
KatalysatorIronHCID 23925—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktHCID 24270770HCID 24270770100,3%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A solution of 4-chloro-N-methyl-3-nitrobenzenesulfonamide (6.35 g, 25.3 mmol) in EtOH (150 mL) and water (50.0 mL) was treated with iron (14.15 g, 253 mmol) and NH4Cl (13.55 g, 253 mmol) and heated at 90° C. for 4 hours before being cooled and filtered through celite. The filter cake was washed with EtOAc and the combined filtrate was filtered again to remove precipitated NH4Cl before being concentrated. The resulting crude material was partitioned between 350 ml EtOAc and 50 ml saturated aqueous NaHCO3. The organic layer was washed with brine, dried over MgSO4, concentrated and subjected to flash column chromatography (330 g silica gel, 0-15% EtOAc/DCM) to afford 3-amino-4-chloro-N-methylbenzenesulfonamide (5.60 g, 100%) as a light yellow crystalline solid. 1H NMR (400 MHz, MeOD) δ ppm 7.39 (d, J=8.28 Hz, 1 H), 7.27 (d, J=2.26 Hz, 1 H), 7.03 (dd, J=8.28, 2.26 Hz, 1 H), 2.54 (s, 3 H). MS 221.0 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859571B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-26c3d12832794095993a78f98c765b3d
Quellennotizuspto-grants-2014_10