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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393144Generated: October 27, 2026

Ethanol → N-(Hex-5-en-1-yl)hex-5-en-1-amine

https://huagongshe.com/reaction/1393144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant3-(Di-5-hexenyl)aminopropionitrileHCID 12136627—
SolventChloroformHCID 6212—
ProductN-(Hex-5-en-1-yl)hex-5-en-1-amineHCID 1564033221%

Reaction Steps

Next, ethanol (8.6 ml) and potassium hydroxide (0.85 g, 13 mmol) were added to 3-(di-5-hexenyl)aminopropionitrile (2.0 g, 8.6 mmol), and the mixture was refluxed for 7.5 hours. The reaction mixture was allowed to stand, and then water (150 ml) and chloroform (150 ml) were added to the reaction mixture. Layers were separated, and the organic layer was dried over sodium sulfate. The organic layer was concentrated under reduced pressure, and the residue was purified by basic silica gel column chromatography to give 0.32 g (21%) of the titled compound as a pale yellow oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345064B2
Source datasetuspto-grants-2008_03
ORD IDord-b0e238bf03ed47fd90d5b496e1dc09a9
Source noteuspto-grants-2008_03