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HRID 430928作成日:2026年10月26日

Methyl iodide → 5-methoxy-1-methyl-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/430928

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Sodium hydrideHCID 24758—
反応物5-Methoxyindole-3-carbaldehydeHCID 82758—
反応物Sodium BicarbonateHCID 516892—
溶媒DimethylformamideHCID 6228—
生成物5-methoxy-1-methyl-1H-indole-3-carbaldehydeHCID 92597399%

反応手順

5-Methoxyindole-3-carboxaldehyde (300 mg, 1.71 mmol) was added in portions over 5 min to a suspension of sodium hydride (82 mg, 2.05 mmol, 60% dispersion in mineral oil) in DMF (8 mL) stirring under argon. The mixture was stirred for 30 min, methyl iodide (0.13 mL, 2.05 mmol) was added and the mixture was stirred for 1 h. Sodium bicarbonate (10%, 40 mL) was added and the mixture was extracted with EtOAc (4×). The combined organic layers were washed with sodium bicarbonate (10%, 2×) and saturated NaCl, dried (MgSO4), filtered and evaporated. Column chromatography of the crude product (50:50 EtOAc:hexanes) afforded 43 (320 mg, 99%) as a light yellow solid; Rf=0.35 (50:50 EtOAc:hexanes); mp=130-132° C.; lit mp=132-133° C.53; 1H NMR (CDCl3): δ 9.95 (s, 1H), 7.79 (d, 1H, J=2.4 Hz), 7.62 (s, 1H), 7.25 (d, J=8.8 Hz), 6.96 (dd, 1H, J=2.4 and 8.9 Hz), 3.90 (s, 3H), 3.85 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06656926B2
出典データセットuspto-grants-2003_12
ORD IDord-07f2ad9f91d446ce89d8ac272f67b7d0
出典メモuspto-grants-2003_12