戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1743396作成日:2026年10月26日

Triethylamine → 6,7-Dimethyl-5-methoxy-3-(methylthio)-1,3-dihydro-2H-indole-2-one

https://huagongshe.com/reaction/1743396

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sulfuryl chlorideHCID 24648—
反応物Methyl (methylthio)acetateHCID 85522—
反応物Proton spongeHCID 88675—
反応物4-Methoxy-2,3-dimethylanilineHCID 11094809—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物6,7-Dimethyl-5-methoxy-3-(methylthio)-1,3-dihydro-2H-indole-2-oneHCID 2223807746%

反応手順

To a solution of methyl (methylthio)acetate (40.8 mL, 317 mmol) in dichloromethane (1100 mL) was added sulfuryl chloride (26.6 mL, 331 mmol) at −78° C., and the mixture was stirred for 15 minutes. Further, a solution of 4-methoxy-2,3-dimethylaniline (41.7 g, 276 mmol) and proton sponge (62.1 g, 290 mmol) in dichloromethane (200 mL) was added dropwise over 1 hour and mixture was stirred at the same temperature for 1 hour. Triethylamine (43 mL, 380 mmol) was added, and the temperature was gradually raised to room temperature. After stirring at room temperature for 2 hours, water was added, the organic layer was washed with an aqueous saturated solution of sodium bicarbonate and saturated brine, dried over sodium sulfate, and the solvent was distilled off under reduced pressure. To the residue was added toluene (300 mL), and the mixture was stirred at reflux for 1 hour. The solvent was distilled off under reduced pressure, which was recrystallized from ethyl acetate to obtain 30.0 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07008940B1
出典データセットuspto-grants-2006_03
ORD IDord-d7c675b9ee8e41cd9e3d5f36d3576b26
出典メモuspto-grants-2006_03