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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218172Generated: October 31, 2026

(1-(4-Fluorophenyl)-1H-indazol-5-yl)methanol → 1-(4-fluorophenyl)-1H-indazole-5-carboxylic acid

https://huagongshe.com/reaction/218172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-(4-Fluorophenyl)-1H-indazol-5-yl)methanolHCID 67005185—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
Product1-(4-fluorophenyl)-1H-indazole-5-carboxylic acidHCID 5962599889%

Reaction Steps

To a stirred solution of (1-(4-fluorophenyl)-1H-indazol-5-yl)methanol (0.45 g, 1.9 mmol) in acetone (10 mL) was added Jones' reagent (3 mL) dropwise at 0° C. The reaction mixture was stirred at rt for 1 hr and concentrated under reduced pressure. Water was added to the residue and the solid that separates out was filtered, washed with water and dried to give 1-(4-fluorophenyl)-1H-indazole-5-carboxylic acid (0.43 g, 1.7 mmol, 89% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198311B2
Source datasetuspto-grants-2012_06
ORD IDord-634776d34bd8431bb1426a48caffe808
Source noteuspto-grants-2012_06