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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 256605Erstellt: 25. Oktober 2026

Triethylamine → N-(2-Chloro-4-methylphenyl)methanesulfonamide

https://huagongshe.com/reaction/256605

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-Chloro-p-toluidineHCID 12007—
EduktMethanesulfonyl chlorideHCID 31297—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2-Chloro-4-methylphenyl)methanesulfonamideHCID 1978560932,3%

Reaktionsschritte

A solution of 2-chloro-4-methylaniline (5.00 g) and triethylamine (3.57 g) in dichloromethane (100 ml) was cooled to 0° C. Methanesulphonyl chloride (4.04 g) was added dropwise and the mixture stirred at ambient temperature overnight. The mixture was then washed with 2N aqueous hydrochloric acid solution (50 ml) and the solvent removed by evaporation. The residue was dissolved in ethyl acetate (75 ml) extracted with 2N aqueous sodium hydroxide solution (2×50 ml). The aqueous phase was acidified with 2N aqueous hydrochloric acid solution and extracted with ethyl acetate (2×75 ml). This was subsequently dried (MgSO4) and the solvent evaporated. Thus was obtained N-(2-chloro-4-methylphenyl)methanesulphonamide (2.5 g, 32%). NMR Spectrum 2.33 (3H, s), 2.97 (3H, s), 6.6 (1H, s), 7.10 (1H, d), 7.25 (1H, s), 7.52 (1H, d).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05258399
Quelldatensatzuspto-grants-1993_11
ORD IDord-0533d51cf27c41d48af9351d24ce8f58
Quellennotizuspto-grants-1993_11