HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → Piperidine-1-propylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-(Piperidin-1-yl)propanenitrile | HCID 12957465 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Piperidine-1-propylamine | HCID 19049 | — |
Reaction Steps
Reaction of piperidine (Aldrich, 8.4 g, 100 mmol) with acrylonitrile (7.96 g, 150 mmol) in ethanol (25 mL), reduction of the resulting piperidinopropionitrile with lithium aluminum hydride (5 g, 125 mmol) in tetrahydrofuran (150 mL), work-up and distillation under reduced pressure as described for Example 3 gave the title compound. Yield: 3 g (21%); bp. 65°-66° (6 Torr); [lit. bp. 110°-115° C. (31 Torr), J. Corse et al., J. Amer. Chem. Soc., 68, 1911 (1946)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05349063 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-f036c09dfb994ae8973e66bcfb8ebc39 |
| Source note | uspto-grants-1994_09 |