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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1384202Erstellt: 26. Oktober 2026

Toluene → 4-Nitrophenyl 2-(4-isobutylphenyl)pyridine-3-sulphonate

https://huagongshe.com/reaction/1384202

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktPotassium FluorideHCID 522689—
Edukt(4-Isobutylphenyl)boronic acidHCID 2773472—
Edukt4-Nitrophenyl 2-chloropyridine-3-sulphonateHCID 21186255—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
Produkt4-Nitrophenyl 2-(4-isobutylphenyl)pyridine-3-sulphonateHCID 2118622855,3%

Reaktionsschritte

Tetrakis(triphenylphosphine)palladium(0) (0.076 g) was added to a deoxygenated mixture of 4-nitrophenyl 2-chloropyridine-3-sulphonate (0.69 g), 4-isobutylphenylboronic acid (0.47 g), potassium fluoride (0.38 g), toluene (15 ml) and water (2.5 ml) and the mixture was stirred and heated under reflux for 24 hours. Water (50 ml) was added and the mixture was extracted with ethyl acetate (2×80 ml). The organic extracts were washed with saturated sodium chloride solution and then combined and dried (MgSO4). Volatile material was removed by evaporation and the residue was purified by gradient elution with dichloromethane/hexane (1:1-1:0 v/v) then dichloromethane/hexane/ethyl acetate (10:9:1 v/v) through a silica gel Mega Bond Elut column followed by recrystallisation from ethyl acetate/hexane to give 4-nitrophenyl 2-(4-isobutylphenyl)pyridine-3-sulphonate (0.50 g), m.p. 123-124° C.; 1H NMR (d6-DMSO): 0.9 (d, 6H), 1.9 (m, 1H), 2.55 (d, 2H), 7.2-7.3 (m, 4H), 7.5 (d, 2H), 7.7 (dd, 1H), 8.2 (d, 2H), 8.4 (dd, 1H), 9.0 (dd, 1H); mass spectrum (+ve FAB, NBA/DMSO): 413 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06258817B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-88689a5c7139437f89a0c28cb08a1090
Quellennotizuspto-grants-2001_07