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HRID 1272736作成日:2026年10月26日

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

https://huagongshe.com/reaction/1272736

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物5-Nitro-3-phenyl-1H-indazoleHCID 617444—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
触媒HCID 178418390HCID 178418390—
生成物3-phenyl-1H-indazole-5-olHCID 2247986228%

反応条件

温度180 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07208513B2
出典データセットuspto-grants-2007_04
ORD IDord-585974251c2b4a6ca14240322bb05e1c
出典メモuspto-grants-2007_04