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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248752Erstellt: 24. Oktober 2026

Pyridine → 4-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl)benzoic acid

https://huagongshe.com/de/reaction/248752

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktSodium HydroxideHCID 14798—
Edukt4-Fluoro-3-(trifluoromethyl)anilineHCID 75377—
Edukt4-(Chlorosulfonyl)benzoic acidHCID 82385—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl)benzoic acidHCID 3699990—

Reaktionsschritte

10 g (55.8 mmol) of 4-fluoro-3-trifluoromethylaniline and 6 ml (74.3 mmol) of pyridine are dissolved in 250 ml of dichloromethane. The mixture is cooled with ice water and, under agitation and exclusion of moisture, 12.7 g (57.6 mmol) of 4-chlorosulfonylbenzoic acid is added in incremental portions. The mixture is stirred overnight; the slurry is combined with 75 ml of 2N sodium hydroxide solution, and the organic phase is separated. The alkaline solution is washed with dichloromethane and then adjusted to pH 2 with hydrochloric acid. The product is taken up in ethyl acetate. The solution is washed with water, dried over sodium sulfate and concentrated to dryness. The title compounds melts at 243-°245° C. after crystallization from ethanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05210290
Quelldatensatzuspto-grants-1993_05
ORD IDord-b639f8a2c482415fbde171d119d57f67
Quellennotizuspto-grants-1993_05