戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 276882作成日:2026年10月25日

1,5-Dibromopentane → 2a-(5-Bromopentyl)-2a, 3,4,5-tetrahydrobenz[cd]indole-2(1H)-one

https://huagongshe.com/reaction/276882

反応式

関与物質

役割名称HCID仕込み量
反応物1,5-DibromopentaneHCID 8100—
反応物Sodium hydrideHCID 24758—
反応物2a,3,4,5-Tetrahydrobenzo[cd]indol-2(1H)-oneHCID 599375—
溶媒DimethylformamideHCID 6228—
生成物2a-(5-Bromopentyl)-2a, 3,4,5-tetrahydrobenz[cd]indole-2(1H)-oneHCID 1554263412.1%

反応手順

2a, 3,4,5-Tetrahydrobenz [cd]indole-2(1H) -one (1.0 g, 5.8 mmol) was dissolved in anhydrous N,N-dimethylformamide (40 ml). Thereto was added sodium hydride (250 mg, 6.3 mmol), and the resulting solution was stirred at a room temperature for 1 hour. The reaction solution was mixed with 1,5-dibromopentane (2.4 ml, 17 mmol) and again stirred for 17 hours. The solvent was evaporated under a reduced pressure, and the thus obtained residue was mixed with ethyl acetate and water. The reaction product was extracted with ethyl acetate, washed with saturated brine and dried with anhydrous sodium sulfate. Then the compound obtained by the evaporation of the solvent under a reduced pressure was separated and purified by a silica gel column chromatography to obtain 230 mg of the title compound (0.70 mmol, 12% in yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355642B1
出典データセットuspto-grants-2002_03
ORD IDord-f44dc5d8d2e24651943c6afd281e9c0f
出典メモuspto-grants-2002_03