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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 731225Erstellt: 24. Oktober 2026

Water → 2-Benzylamino-5-nitro-benzenesulfonamide

https://huagongshe.com/de/reaction/731225

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBenzylamineHCID 7504—
Edukt2-Chloro-5-nitrobenzenesulfonamideHCID 66784—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-Benzylamino-5-nitro-benzenesulfonamideHCID 2485839783,4%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

A solution of 2-chloro-5-nitro-benzenesulfonamide (20 g, 84.52 mmol) in acetonitrile (169 mL) was treated with benzylamine (13.85 mL, 126.78 mmol), diisopropyl ethylamine (29.44 mL, 169.04 mmol) and stirred for 16 h at 55° C. The reaction was cooled to 25° C., poured into water (1.0 L) then placed in an ice bath while stirring. After 4 h a precipitate was filtered off and washed with the mother liquor to afford the desired product, 2-benzylamino-5-nitro-benzenesulfonamide (21.65 g, 70.45 mmol, 83.3%) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ: 4.64 (2H, d, J=4.6 Hz), 6.81 (1H, d, J=9.4 Hz), 7.23-7.44 (6H, m), 7.77 (2H, bs), 8.11 (1H, dd, J1=9.4 Hz, J2=2.3 Hz), 8.49 (1H, d, J=3.1 Hz). LC-MS (ESI) calcd for C13H13N3O4S 307.06, found 308.2 [M+H+] (100%), 615.2 [2M+H+] (81%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07582626B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-7471437e19c74501b00ff0a0c15570ab
Quellennotizuspto-grants-2009_09