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HRID 55921作成日:2026年10月23日

Indole → 3-Naphthoylindole

https://huagongshe.com/ja/reaction/55921

反応式

関与物質

役割名称HCID仕込み量
反応物IndoleHCID 798—
反応物Ammonium ChlorideHCID 25517—
反応物1-Naphthalenecarbonyl chlorideHCID 70146—
反応物HCID 178418573HCID 178418573—
溶媒Diethyl EtherHCID 3283—
生成物3-NaphthoylindoleHCID 1035582591%

反応手順

To a cooled solution of indole (5.85 g, 50 mmol) in ether (50 ml) under nitrogen was added slowly a solution of methylmagnesium bromide (3M) in ether (17.5 ml). After addition, the reaction mixture was warmed up to room temperature and stirred for 2 h at room temperature. Then the mixture was cooled down again to 0° C., and to it was added slowly with stirring a solution of 1-naphthoylchloride (9.5 g, 50 mmol) in ether (50 ml). The resulting mixture was warmed up to room temperature and stirred for 2 h at room temperature followed by slow addition of saturated ammonium chloride solution (375 ml). The mixture was then stirred overnight at room temperature. A white solid was formed, filtered, washed by ether and dried under high vacuum to give 3-(1-naphthoyl)-1H-Indole 1 (12.3 g, 91%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434687B2
出典データセットuspto-grants-2016_09
ORD IDord-8a303a3c232549e4839a627077ca7aa6
出典メモuspto-grants-2016_09