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HRID 352355作成日:2026年10月26日

Methyl iodide → 1-Acetyl-6-bromo-5-methoxyindoline

https://huagongshe.com/reaction/352355

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物1-(6-Bromo-5-hydroxy-2,3-dihydro-1H-indol-1-yl)ethan-1-oneHCID 21948380—
溶媒DimethylformamideHCID 6228—
生成物1-Acetyl-6-bromo-5-methoxyindolineHCID 2194837588.1%

反応手順

A stirred solution of 1-acetyl-6-bromoindolin-5-ol (Tetrahedron 1973, 29(8), 1115; 40 g, 0.15 mole) in DMF (500 ml) was treated with K2CO3 (61 g, 0.45 mole) and iodomethane (11.7 ml, 0.19 mole) and maintained at room temperature for 20 h, then concentrated under vacuum to 200 ml. The residue was treated with water (200 ml) and the precipitate filtered off, dried and recrystallised from EtOAc to afford the title compound as a white solid (35.7 g, 85%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747030B1
出典データセットuspto-grants-2004_06
ORD IDord-1209a2796f0e4beea1373760462eba3d
出典メモuspto-grants-2004_06