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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349589Generated: October 25, 2026

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

https://huagongshe.com/reaction/1349589

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 (250 mg, 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 numberUS07211594B2
Source datasetuspto-grants-2007_05
ORD IDord-9dfcc6c361bf4876b56561f4b3da6afe
Source noteuspto-grants-2007_05