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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423095Generated: November 1, 2026

1-{3-Fluoro-4-[(phenylmethyl)oxy]phenyl}-1H-indazol-4-ol → 1-(3-Fluoro-4-hydroxyphenyl)-1H-indazol-4-ol

https://huagongshe.com/reaction/2423095

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-{3-Fluoro-4-[(phenylmethyl)oxy]phenyl}-1H-indazol-4-olHCID 136085246—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product1-(3-Fluoro-4-hydroxyphenyl)-1H-indazol-4-olHCID 13590694985.2%

Reaction Steps

A solution of 1-{3-fluoro-4-[(phenylmethyl)oxy]phenyl}-1H-indazol-4-ol (D39) (3.79 g, 11.3 mmol) in ethyl acetate (150 mL) was hydrogenated overnight at room temperature and pressure over 10% palladium on charcoal (700 mg). The mixture was filtered through a pad of celite, washed with ethyl acetate and the resulting filtrate was concentrated in vacuo. The product was purified by silica gel chromatography eluting with 5-80% ethyl acetate in hexane. The product was then triturated with hexane and the product collected by filtration and dried in a vacuum oven to yield the title compound (Ela) (2.35 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960563B2
Source datasetuspto-grants-2011_06
ORD IDord-d0264642baa549768961c8c08ab0f303
Source noteuspto-grants-2011_06