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HRID 11439作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/11439

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 residue was purified by silica gel column chromatography to give 2.2 g (66%) of 3-(di-5-hexenyl)aminopropionitrile as a colorless oily matter.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098226B2
出典データセットuspto-grants-2006_08
ORD IDord-5be7de404eea4fd0bdb5fb8ce7e9a3b1
出典メモuspto-grants-2006_08