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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1167241Erstellt: 26. Oktober 2026

Dimethylamine → 2,4-dimethyl-5-nitro (N,N-dimethyl)benzenesulfonamide

https://huagongshe.com/reaction/1167241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
Edukt4-Nitro-m-xyleneHCID 6991—
EduktChlorosulfonic acidHCID 24638—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,4-dimethyl-5-nitro (N,N-dimethyl)benzenesulfonamideHCID 983493537%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

In a dry flask under argon filled with 2,4-dimethyinitrobenzene (1.0 g, 6.61 mmol), chlorosulfonic acid (5 mL) was added dropwise. The resulting solution was stirred at 130° C. for 4 h, and then the mixture was poured slowly onto ice. A light brown precipitate formed and was isolated by filtration. The solid was dissolved in methanol (20 mL), and dimethylamine (3 mL) was added with stirring. After 15 min, the reaction mixture was diluted with methylene chloride and 1 M HCl. The layers were separated, and the organics were dried and concentrated. Purification of the residue by flash chromatography (15% ethyl acetate/hexanes) provided 2,4-dimethyl-5-nitro (N,N-dimethyl)benzenesulfonamide (626 mg, 37%) as a white solid. Anal. Calcd for C10H14N2O4S: C, 46.50; H, 5.46; N, 10.85. Found: C, 46.68; H, 5.25; N, 10.71.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06617357B2
Quelldatensatzuspto-grants-2003_09
ORD IDord-cfcef51d76e14bb9b49ffe780ca6a967
Quellennotizuspto-grants-2003_09