戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1526949作成日:2026年10月27日

Dimethyl Sulfoxide → ethyl 2-methyl-1H-indole-3-carboxylate

https://huagongshe.com/reaction/1526949

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Ethyl AcetoacetateHCID 8868—
反応物Cesium carbonateHCID 10796—
反応物2-IodoanilineHCID 11995—
触媒HCID 178419072HCID 178419072—
溶媒WaterHCID 962—
生成物ethyl 2-methyl-1H-indole-3-carboxylateHCID 407235815.1%

反応条件

温度100 °C

反応手順

To a mixed solution of dimethyl sulfoxide and water (20 mL), 2-iodobenzenamine (3.0 g, 13.7 mmol), ethyl 3-oxobutanoate (2.0 g, 15.1 mmol), copper(I) oxide (0.2 g, 1.4 mmol) and cesium carbonate (4.5 g, 13.7 mmol) was added. The mixture was stirred at 100° C. for 9 hours under nitrogen gas atmosphere. The reaction mixture was filtered through a pad of celite. The filtrate was diluted with water and extracted with ethyl acetate. The organic phase was concentrated in vacuo, and then the residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=5:1) to give ethyl 2-methyl-1H-indole-3-carboxylate as a light yellow solid (0.42 g, 15%). 1H NMR (300 MHz, CDCl3): δ 8.12-8.09 (m, 1H), 7.31-7.16 (m, 3H), 4.40 (q, J=6.9 Hz, 2H), 2.77 (s, 3H), 1.45 (t, J=6.9 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09085583B2
出典データセットuspto-grants-2015_07
ORD IDord-bb1e46f6229547b2979abf4b7300b792
出典メモuspto-grants-2015_07