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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 246616Erstellt: 26. Oktober 2026

Potassium Hydroxide → 5-(difluoromethoxy)-3-iodo-1-methyl-1H-indazole

https://huagongshe.com/reaction/246616

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktBromodifluoromethyl diethylphosphonateHCID 144101—
EduktAcetone cardiceHCID 18522661—
Edukt3-Iodo-1-methyl-1H-indazol-5-olHCID 71279721—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-(difluoromethoxy)-3-iodo-1-methyl-1H-indazoleHCID 7127954453%

Reaktionsschritte

Diethyl bromodifluoromethylphosphonate (9 g, 10.9 mmol) was added in one portion to a cooled (dry ice-acetone bath) solution of 3-iodo-1-methyl-1H-indazol-5-ol (3 g, 37.8 mmol) and KOH (15 g, 267 mmol) in CH3CN (50 mL) and H2O (50 mL) with stirring, the reaction mixture was warmed to room temperature and stirred for 0.5 h, the mixture was diluted with EtOAc (50 mL), The organic layer was washed with H2O (50 mL), brine (100 mL), dried over Na2SO4 and concentrated under reduced pressure, the residue was purified by column chromatography (silica gel, 200-300 mesh, eluting with petroleum ether/EtOAc=3:1) to give 5-(difluoromethoxy)-3-iodo-1-methyl-1H-indazole (1.85 g, 53%) as a white solid. LCMS: (M+H)+=325; 1H NMR (300 MHz, CDCl3), δ 7.36-7.33 (m, 1H), 7.28-7.23 (m, 1H), 7.19 (s, 1H), 6.53 (t, 1H, J=73.5 Hz), 4.09 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658646B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-0b6f2c2e918a4c72aca5771957abe10a
Quellennotizuspto-grants-2014_02