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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18382생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/18382

반응식

참여 물질

역할이름HCID투입량
반응물3-AminopropionitrileHCID 1647—
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물6-Bromo-1-hexeneHCID 75906—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물3-(Di-5-hexenyl)aminopropionitrileHCID 1213662767%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741346B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ac0a6b6c606f4b0f9a11ff9d59f587bb
출처 메모uspto-grants-2010_06