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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183097Generated: October 25, 2026

Ethyl Acetate → 3-phenyl-1H-indazole-5-ol

https://huagongshe.com/reaction/2183097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant5-Nitro-3-phenyl-1H-indazoleHCID 617444—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
CatalystHCID 178418390HCID 178418390—
Product3-phenyl-1H-indazole-5-olHCID 2247986228%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a solution of 5-nitro-3-phenyl-1H-indazole (1.0 g, 4.2 mmol) in ethyl acetate (80 mL) was added palladium on activated carbon (Pd/carbon) then the reaction was subjected to an atmosphere of hydrogen. The reaction was stirred for 3 days when the Pd/carbon was filtered off and the solution concentrated to an oil under vacuo. The oil was then taken up in H2SO4 (6 mL) and water (60 mL) and the suspension was heated in a bomb to 180° C. for 2 days. The reaction was then cooled to room temperature, quenched with NaHCO3 (100 mL) and extracted with ethyl acetate (3×30 mL). The organic layers were combined and dried (Na2SO4) and concentrated to recover the title compound (250mg, 28% yield). 1H NMR (CDCl3) δ 13.0 (s, 1H), 9.20 (s, 1H), 7.91 (s, 1H), 7.88 (s, 1H), 7.50 (t, 2H), 7.41 (d, 1H), 7.36 (t, 1H), 7.28 (s, 1H), 6.96 (dd, 1H); ES-MS (m/z) 195 [M+1]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897231B2
Source datasetuspto-grants-2005_05
ORD IDord-0bc1bc630e7c4be2ba990b441554481b
Source noteuspto-grants-2005_05