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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246616Generated: October 26, 2026

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

https://huagongshe.com/reaction/246616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantBromodifluoromethyl diethylphosphonateHCID 144101—
ReactantAcetone cardiceHCID 18522661—
Reactant3-Iodo-1-methyl-1H-indazol-5-olHCID 71279721—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product5-(difluoromethoxy)-3-iodo-1-methyl-1H-indazoleHCID 7127954453%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-0b6f2c2e918a4c72aca5771957abe10a
Source noteuspto-grants-2014_02