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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2183097Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2183097

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt5-Nitro-3-phenyl-1H-indazoleHCID 617444—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
KatalysatorHCID 178418390HCID 178418390—
Produkt3-phenyl-1H-indazole-5-olHCID 2247986228%

Reaktionsbedingungen

Temperatur180 °C

Reaktionsschritte

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]−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06897231B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-0bc1bc630e7c4be2ba990b441554481b
Quellennotizuspto-grants-2005_05