HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → 4-(3-Cyanopropyl)-1-piperidinecarboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 4-(3-Bromopropyl)-1-piperidinecarboxaldehyde | HCID 20239768 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(3-Cyanopropyl)-1-piperidinecarboxaldehyde | HCID 20239759 | 61.5% |
Reaction Steps
4-(3-Bromopropyl)-1-piperidinecarboxaldehyde (60 g, 0.256M) and NaCN (25 g) in ethanol (600 ml) was refluxed for 7 hours, Solvent was removed, added water (300-400 ml) and extracted with CH2Cl2 (4×200 ml). The extracts, dried over Na2SO4 was stripped to dryness which was purified on silica gel columns, eluted with ethylacetate-hexane (8:2 parts by volume) to yield 4-(3-cyanopropyl)-1-piperidinecarboxaldehyde (28.4 g, 61% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04605744 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-1f45f64f0199471fb4d6fa2609bd7e29 |
| Source note | uspto-grants-1986_08 |