HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-(Hex-5-en-1-yl)hex-5-en-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-(Di-5-hexenyl)aminopropionitrile | HCID 12136627 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(Hex-5-en-1-yl)hex-5-en-1-amine | HCID 15640332 | 21% |
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 obtained mixture was refluxed for 7.5 hours. The reaction mixture was allowed to stand, then water (150 ml) and chloroform (150 ml) were added to the reaction mixture. After separation, the organic layer was dried over sodium sulfate and concentrated under reduced pressure, and the resulting residue was purified by basic silica gel column chromatography to give the target compound (0.32 g, 21%) as a pale yellow oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741346B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-83150b480f524dde80da8571a47199d3 |
| Source note | uspto-grants-2010_06 |