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HRID 2214751作成日:2026年10月25日

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

https://huagongshe.com/reaction/2214751

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%). MH+ 270/272.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07109201B2
出典データセットuspto-grants-2006_09
ORD IDord-5f997226f28c48008664d4de881b219d
出典メモuspto-grants-2006_09