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HRID 235406生成日期:2026年10月23日

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 7-(3-chloropropoxy)-1H-indole

https://huagongshe.com/zh-CN/reaction/235406

反应方程式

参与物

角色名称HCID投料
反应物聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
反应物1-溴-3-氯丙烷HCID 8006—
反应物氢化钠HCID 24758—
反应物7-羟基吲哚HCID 2737651—
溶剂N,N-二甲基甲酰胺HCID 6228—
产物7-(3-chloropropoxy)-1H-indoleHCID 15384964—

反应步骤

To a stirred suspension of sodium hydride (0.8 g, 17 mmol of a 50% oil dispersion) in dimethylformamide (20 ml), under nitrogen, was added dropwise 7-hydroxyindole (2.1 g, 15.7 mmol) in dimethylformamide (20 ml). After complete addition, the reaction was stirred at ambient temperature for 0.5 hour and then cooled to 15° C. To this cooled solution was added, dropwise, 1-bromo-3-chloropropane (2.5 g, 15.7 mmol) in dimethylformamide (5 ml). The reaction was then stirred at ambient temperature for 16 hours. The reaction was poured into water, and the aqueous suspension extracted with ethyl acetate. The ethyl acetate was washed with water, dried (MgSO4), and the solvent was concentrated to afford a dark brown oil. Following flash chromatography on silica gel, 7-(3-chloropropoxy)indole was obtained as a colorless oil, 1.0 g.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05597842
来源数据集uspto-grants-1997_01
ORD IDord-d45e6cffcb844f18b8d7ab88dfa912d2
来源说明uspto-grants-1997_01