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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2079892Erstellt: 24. Oktober 2026

Sodium Bicarbonate → 4-(6-nitro-1H-indol-3-yl)-benzonitrile

https://huagongshe.com/de/reaction/2079892

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
EduktTetrabutylammonium FluorideHCID 2724141—
Edukt4-(1-benzenesulfonyl-6-nitro-1H-indol-3-yl)-benzonitrileHCID 57442242—
LösungsmittelAcetoneHCID 180—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(6-nitro-1H-indol-3-yl)-benzonitrileHCID 57442197—

Reaktionsschritte

Add 100 mL of 1 M TBAF in THF to a slurry of 4-(1-benzenesulfonyl-6-nitro-1H-indol-3-yl)-benzonitrile 8 (14.3 g, 35 mmol) in 50 mL of THF. Monitor the reaction by TLC. If starting material remains add more 1 M TBAF in THF until the reaction is complete. Pour reaction mixture into 200 mL of saturated aqueous sodium bicarbonate and then extract the resulting solution 3× with EtOAc. Combine the organic extracts and wash the extracts with saturated aqueous bicarbonate, water (2×), brine. Dry the resulting organic solution over Na2SO4, filter, and then remove the organic solvent to provide a solid. Redisolve the solid in ˜400 mL of acetone with heating and then add ˜100 mL hexanes until a precipitate forms. Let the solution cool and then collect the precipitate. Concentrate the filtrates and redisolve in ˜300 mL of 50% acetone/hexanes with heating. Let the solution cool and then place in a freezer at −20° C. overnight. Collect the crystals that form. The combined yield of the title compound is 6.71 g, 25.5 mmol, 72%. LRMS (API ES−)=262.0 (M−1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07932284B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-57336213eff141c2b05476d1b1da5eae
Quellennotizuspto-grants-2011_04