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HRID 18382作成日:2026年10月25日

3-Aminopropionitrile → 3-(Di-5-hexenyl)aminopropionitrile

https://huagongshe.com/reaction/18382

反応式

関与物質

役割名称HCID仕込み量
反応物3-AminopropionitrileHCID 1647—
反応物Sodium IodideHCID 5238—
反応物Potassium CarbonateHCID 11430—
反応物6-Bromo-1-hexeneHCID 75906—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物3-(Di-5-hexenyl)aminopropionitrileHCID 1213662767%

反応手順

N,N-Dimethylformamide (28 ml) was added to 3-aminopropionitrile (0.98 g, 14 mmol), and the mixture was stirred at room temperature. 6-Bromo-1-hexene (5.0 g, 31 mmol), sodium iodide (11 g, 73 mmol) and potassium carbonate (5.8 g, 42 mmol) were added to the mixture, and the whole was stirred overnight. The reaction mixture was diluted with diethyl ether (100 ml), and the whole was washed with water (100 ml, twice) and saturated brine (50 ml) successively. The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to give 3-(di-5-hexenyl)aminopropionitrile (2.2 g, 66%) as a colorless oily matter.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741346B2
出典データセットuspto-grants-2010_06
ORD IDord-ac0a6b6c606f4b0f9a11ff9d59f587bb
出典メモuspto-grants-2010_06