Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 859673Erstellt: 24. Oktober 2026

Methanesulfonyl chloride → N-(4-bromo-2-ethylphenyl)methanesulfonamide

https://huagongshe.com/de/reaction/859673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonyl chlorideHCID 31297—
Edukt4-Bromo-2-ethylanilineHCID 2801283—
LösungsmittelPyridineHCID 1049—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(4-bromo-2-ethylphenyl)methanesulfonamideHCID 646915281%

Reaktionsschritte

4-Bromo-2-ethyl-aniline (2 mL, 14 mmol) dissolved in anhydrous pyridine (35 mL) at toom temperature was treated with methylsulfonyl chloride (1.3 mL, 16.8 mmol). The reaction was stirred at that temperature for 15 hours before it was diluted with EtOAc. The mixture was washed with H2O, brine and dried over MgSO4. The solvent was removed in vacuo and the residue was purified with flash chromatography (SiO2, 5–30% EtOAc in hexanes) to afford the desired product (3.1 g, 81% yield). 1H NMR (300 MHz, CDCl3): δ 1.25 (t, J=7.5 Hz, 3 H), 2.61–2.68 (m, 2 H), 3.02 (s, 3 H), 6.36 (s, 1 H), 7.36–7.39 (m, 3 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07151105B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-389a00c858154614be5cd1adf398aead
Quellennotizuspto-grants-2006_12