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HRID 217141作成日:2026年10月26日

Pyrazole → 1-(5-Bromo-3-fluoro-2-nitro-phenyl)-1H-pyrazole

https://huagongshe.com/reaction/217141

反応式

関与物質

役割名称HCID仕込み量
反応物PyrazoleHCID 1048—
反応物Sodium hydrideHCID 24758—
反応物5-Bromo-1,3-difluoro-2-nitrobenzeneHCID 21335487—
溶媒TetrahydrofuranHCID 8028—
生成物1-(5-Bromo-3-fluoro-2-nitro-phenyl)-1H-pyrazoleHCID 6700464886%

反応条件

温度0 °C

反応手順

To a suspension of sodium hydride (44 mg, 1.1 mmol, 60% oil dispersion) in THF (4 mL), stirred at 0° C., was added a solution of pyrazole (72 mg, 1.05 mmol) in THF (1 mL). The resulting mixture was stirred at 0° C. for 5 minutes and a solution of 5-bromo-1,3-difluoro-2-nitro-benzene (238 mg, 1 mmol) in THF (1 mL) was added. The mixture was stirred at room temperature for 1 hour, quenched by addition of water (1 mL), then partitioned between water (20 mL) and ethyl acetate (50 mL). The organic layer was washed with brine, dried (MgSO4), and concentrated in vacuo. The residue was purified by column chromatography over silica gel eluted with ethyl acetate:hexanes (1:6), to afford 240 mg (86%) of the title compound. 1H NMR (CDCl3) δ 6.55 (t, 1H), 7.45 (d, 1H), 7.60 (s, 1H), 7.80 (m, 2H). MS M+1 287, M+1+2 289.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193352B2
出典データセットuspto-grants-2012_06
ORD IDord-18cf073f84af497e87c3739ab11ab8f0
出典メモuspto-grants-2012_06