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HRID 16628作成日:2026年10月24日

Benzyl Bromide → 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde

https://huagongshe.com/ja/reaction/16628

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物2-methyl-5-nitro-1H-indole-3-carbaldehydeHCID 609359—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehydeHCID 283825383.2%

反応手順

To a solution of 2-methyl-5-nitro-1H-indole-3-carboxaldehyde (500 mg, 2.45 mmol) in DMF (5 ml) was added potassium carbonate (1.0 g, 7.35 mmol) and benzyl bromide (0.44 ml, 3.68 mmol). The mixture was stirred at room temperature for 4 h, diluted with EtOAc, washed with H2O, brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was triturated with Et2O-hexane to yield 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde (Compound 50) as a yellow solid (600 mg, 83%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737173B2
出典データセットuspto-grants-2010_06
ORD IDord-02e4b9ab0bf74da998fa4be994fe94f7
出典メモuspto-grants-2010_06