HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-acetyl-5-oxohexanenitrile → HCID 18963356, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-acetyl-5-oxohexanenitrile | HCID 423784 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18963356 | HCID 18963356 | — |
Reaction Steps
A solution of 4,4-diacetylbutyronitrile (15.3 g, 0.1 mole) in ethyl alcohol (50 ml) over Raney nickel (2 g) was hydrogenated at room temperature and three atmospheres pressure. After hydrogen uptake had ceased, the catalyst was filtered off and the filtrate concentrated under reduced pressure to give 3-acetyl-2-methyl-1,4,5,6-tetrahydropyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05352793 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-538607f49d3848078520479147bc6f28 |
| Source note | uspto-grants-1994_10 |