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HRID 55924作成日:2026年10月27日

5-Methoxyindole → 5-methoxy-3-(1-naphthoyl)-1H-indole

https://huagongshe.com/reaction/55924

反応式

関与物質

役割名称HCID仕込み量
反応物5-MethoxyindoleHCID 13872—
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5-methoxy-3-(1-naphthoyl)-1H-indoleHCID 6815928775%

反応手順

To a cooled solution at 0° C. of 5-methoxy-1H-indole 3 (7.4 g, 50 mmol) in diethyl ether (150 ml) under nitrogen was added dropwise a solution of methylmagnesium bromide (3M) in diethyl ether (17.5 ml) and the mixture was stirred for 2 h at room temperature. The solution was then cooled at 0° C. and to this solution was added a solution of 1-naphthoylchloride (9.5 g, 50 mmol) in diethyl ether (100 ml) dropwise over a period of 15 min. After the addition was completed the solution was warmed up at room temperature and stirred for 2 h followed by slow addition of saturated ammonium chloride solution (375 ml) and stirred overnight. The white solid formed was filtered, washed by ether and dried under high vacuum to give 5-methoxy-3-(1-naphthoyl)-1H-indole 4 (11.3 g, 75%).

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-fe93391650c3489caaf5e02e57804c70
出典メモuspto-grants-2016_09