Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18382Generated: October 26, 2026

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

https://huagongshe.com/reaction/18382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminopropionitrileHCID 1647—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromo-1-hexeneHCID 75906—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product3-(Di-5-hexenyl)aminopropionitrileHCID 1213662767%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741346B2
Source datasetuspto-grants-2010_06
ORD IDord-ac0a6b6c606f4b0f9a11ff9d59f587bb
Source noteuspto-grants-2010_06