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HRID 33336作成日:2026年10月24日

Dimethylformamide → 2-(4-chloro-phenyl)-3-formyl-1H-indole-4-carboxylic acid methyl ester

https://huagongshe.com/ja/reaction/33336

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Phosphorus oxychlorideHCID 24813—
反応物2-(4-Chloro-phenyl)-1H-indole-4-carboxylic acid methyl esterHCID 18340002—
溶媒DichloromethaneHCID 6344—
生成物2-(4-chloro-phenyl)-3-formyl-1H-indole-4-carboxylic acid methyl esterHCID 18340003—

反応条件

温度0 °C

反応手順

Phosphorous oxychloride (0.42 g, 2.71 mmol) was added to DMF (0.99 g, 13.57 mmol) at 0° C. The resulting colorless solution was added dropwise to a solution of 2-(4-chloro-phenyl)-1H-indole-4-carboxylic acid methyl ester (0.52 g, 1.81 mmol) in 10 mL dry CH2Cl2 at 0° C. The reaction was stirred at 0° C. for 10 min then quenched by addition of 5 mL 2 M NaOAc(aq). The layers were separated and the aqueous layer extracted once with CH2Cl2. The combined organic layers were dried (MgSO4) then concentrated in vacuo leaving anorange oil which crystallized on standing. The crystals were rinsed with CH2Cl2 then dried in vacuo to yield 2-(4-chloro-phenyl)-3-formyl-1H-indole-4-carboxylic acid methyl ester, 231 mg (41%) as an off-white solid: m.p. 221-222° C.; 1H NMR (300 MHz, d6-DMSO) δ 3.93 (s, 3H), 7.49 (app t, J=7.5 Hz, 1H), 7.71 (m, 4H), 7.94 (d, J=7.8 Hz, 2H), 9.71 (s, 1H), 13.67 (br s, 1H). MS (electrospray, [M−H]) 312.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429578B2
出典データセットuspto-grants-2008_09
ORD IDord-5395efbbbbf94486a8c3769c04995d3e
出典メモuspto-grants-2008_09