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HRID 1460275作成日:2026年10月27日

Benzene → 7-Piperidinoheptanenitrile

https://huagongshe.com/reaction/1460275

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物ChloroformHCID 6212—
反応物PiperidineHCID 8082—
反応物Heptanenitrile, 7-bromo-HCID 88737—
溶媒Diethyl EtherHCID 3283—
生成物7-PiperidinoheptanenitrileHCID 15030043—

反応手順

In a flask equipped with a dropping funnel and a cooler was placed a mixture of 8.94 g of piperidine, 7.7 ml of benzene and 1.5 ml of chloroform. The mixture was refluxed by heating, and to the mixture was dropwise added 9.50 g of 7-bromoheptanenitrile. After the addition was complete, the mixture was further refluxed by heating for 4 hours and then cooled under ambient condition. To the mixture was added ether, and the resulting mixture was stirred for a while. The reaction mixture was filtered to remove insolubles. The insolubles were washed with ether. The filtrate and washings were combined and concentrated under reduced pressure. The residue was distilled under reduced pressure to give 7-piperidinoheptanenitrile as a colorless oil, yield: 8.92 g (theoretical yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05070196
出典データセットuspto-grants-1991_12
ORD IDord-31e562da7b7d43b5894ec849e8bcd488
出典メモuspto-grants-1991_12