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HRID 56237作成日:2026年10月24日

Diiodomethane → 3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrile

https://huagongshe.com/ja/reaction/56237

反応式

関与物質

役割名称HCID仕込み量
反応物DiiodomethaneHCID 6346—
反応物3-CyanophenolHCID 13394—
反応物Sodium hydrideHCID 24758—
反応物6-Nitro-1H-indoleHCID 78502—
溶媒DimethylformamideHCID 6228—
生成物3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrileHCID 9003044751%

反応手順

To a mixture of NaH (3.0 g, 75.0 mmol, 60%) in DMF (20 mL) were added a solution of 6-nitro-1H-indole (4.86 g, 30.0 mmol) in DMF (10 mL) and a solution of 3-hydroxybenzonitrile (3.57 g, 30.0 mmol) in DMF (10 mL) at 0° C. and the mixture was stirred at rt for 2 h. To the reaction mixture was added a solution of diiodomethane (7.5 mL, 90.0 mmol) in DMF (10 mL) slowly without light and the mixture was stirred at rt for 20 h. The mixture was then quenched with water and filtered. The filtrate was extracted with DCM (30 mL×6) and the combined organic layers were washed with brine (50 mL×3), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (4.47 g, 51%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434695B2
出典データセットuspto-grants-2016_09
ORD IDord-4ac7af751afe4a0c8814018ded4486d1
出典メモuspto-grants-2016_09