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HRID 703235作成日:2026年10月26日

Sodium Hydroxide → 1-(5-Methoxy-2-methyl-1H-indol-3-yl)ethanone

https://huagongshe.com/reaction/703235

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Phosphorus oxychlorideHCID 24813—
反応物DimethylacetamideHCID 31374—
反応物5-Methoxy-2-methylindoleHCID 70642—
溶媒WaterHCID 962—
生成物1-(5-Methoxy-2-methyl-1H-indol-3-yl)ethanoneHCID 60482367.2%

反応条件

温度0 °C

反応手順

Dimethylacetamide (17.5 ml, 188.4 mmol) is added dropwise with stirring to phosphorous oxychloride (12.9 ml, 138.2 mmol) at 0° C. Stirring is maintained for 45 minutes, at which time the bath is removed and 5-methoxy-2-methylindole (20.25 g, 125.6 mmol) in 15 ml of dimethylacetamide is added dropwise over a period of 75 minutes. The resulting mixture is warmed to 40°-45° C. for 4 hours. The reaction mixture is cooled to 0° C., and 100 g of ice water is added followed by dropwise addition of a solution of sodium hydroxide (50 g) in water (75 ml). The first 1/3 of this sodium hydroxide solution is added slowly and the remainder is added quickly. The exothermic reaction is quickly warmed to boiling for 15 minutes, cooled to room temperature and refrigerated overnight. The resulting crystals are collected by filtration and rinsed four times with water. Recrystallization from ethanol/water gives 17.2 g (67.2%) of pure 1-(5-methoxy-2-methyl-1H-indol-3-yl)ethanone; mp 229.0°-230.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04981865
出典データセットuspto-grants-1991_01
ORD IDord-aaba1a13538846a08358f100659875e4
出典メモuspto-grants-1991_01