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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1272736Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1272736

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 (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]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07208513B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-585974251c2b4a6ca14240322bb05e1c
Quellennotizuspto-grants-2007_04