HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → 2-Nonen-1-ol, (2Z)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Non-2-yn-1-ol | HCID 80017 | — |
| Catalyst | Lindlars catalyst | HCID 131709914 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Nonen-1-ol, (2Z)- | HCID 5365027 | 22.8% |
Reaction Steps
2-Nonyn- 1-ol (20 g, 0.4 mole) in 200 ml methyl alcohol is hydrogenated in a Parr bomb using a Lindlar catalyst (0.5 g Pd/BaSO4) and quinoline (0.5 g). The hydrogenation was monitored by gas liquid partition chromatography on diethylene glycol succinate. Hydrogenation is stopped when the concentration of the acetylenic alcohol equals that of the saturated alcohol. The hydrogenation mixture is filtered, diluted with water and extracted with ether. The ether extract is dried over anhydrous sodium sulfate, concentrated and distilled to yield 13 g of cis-2-nonen-1-ol, b.p. 60°-64°C/0.5 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03962321 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-a0faf13214f74682a1fc1f67ec67e44f |
| Source note | uspto-grants-1976_06 |