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HRID 1633591作成日:2026年10月25日

Piperidine → 1-(3-Nitrophenyl)piperidine

https://huagongshe.com/reaction/1633591

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物1-Fluoro-3-nitrobenzeneHCID 9823—
溶媒WaterHCID 962—
生成物1-(3-Nitrophenyl)piperidineHCID 1476527593.7%

反応条件

温度110 °C

反応手順

A mixture of 3-fluoronitrobenzene (10.0 g, 70.9 mmol) and piperidine (14 ml, 141 mmol) was stirred at 110° C. for 3 days. After cooling water (200 ml) was added and the mixture was extracted with dichloromethane (3×100 ml). The combined organic extracts were washed with saturated aqueous sodium carbonate, dried over sodium sulfate and evaporated to dryness to leave 1-(3-nitrophenyl)piperidine (13.7 g, 93%) as an oil. This oil was dissolved in ethanol (150 ml) and was hydrogenated at ambient pressure using palladium on activated carbon as the catalyst to yield 2a (11.7 g, 100%) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06503925B1
出典データセットuspto-grants-2003_01
ORD IDord-5503d3ab1790445fb54a89a117deb5a7
出典メモuspto-grants-2003_01