Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6882Erstellt: 23. Oktober 2026

Citric Acid → N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide

https://huagongshe.com/de/reaction/6882

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCitric AcidHCID 311—
EduktNitric AcidHCID 944—
EduktSulfuric AcidHCID 1118—
Edukt4-Fluorobenzenesulfonyl chlorideHCID 9588—
EduktCyclopropylamineHCID 69828—
EduktDiisopropylethylamineHCID 81531—
ProduktN-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamideHCID 846927392%

Reaktionsschritte

To a solution of fuming nitric acid (8 mL) and conc. H2SO4 (16 mL), was added 4-fluorobenzenesulfonyl chloride (1.3 g, 6.7 mmol) in small portions. The mixture was stirred at RT for 2 h. and then poured onto crushed ice (60 g) and extracted with dichloromethane (2×). The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated. The residue was dissolved in CH2Cl2 (30 mL) cooled to −40° C. and cyclopropylamine (388 mg, 6.8 mmol), followed by DIPEA (8 mmol) were added. After stirring at −40° C. for 2 h, the mixture was poured on 5% citric acid solution and extracted with dichloromethane. The organic layer was separated, and passed through a short pad of silica gel and concentrated in vacuo to afford N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide (1.6 g, 92%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084160B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-462377d8589748f69115599778a6a316
Quellennotizuspto-grants-2006_08