HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Quinolinecarboxaldehyde → 1-(Quinolin-4-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Quinolinecarboxaldehyde | HCID 78072 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(Quinolin-4-yl)ethanol | HCID 5314755 | 64.9% |
Reaction Steps
To 4-quinolinecarbaldehyde (2 g, 12.73 mmol) in 20 ml anhydrous ether, MeLi (1.4M, 10 ml, 13.9 mmol) was added dropwise over a period of five minutes at 0° C. The reaction mixture was stirred at room temperature for 3 hours. The solution was partitioned between ether (20 ml) and water (10 ml). The organic layer was dried over sodium sulfate, filtered and concentrated to give 1.43 g (59%) of the product which was then used as such for the subsequent step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777426B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-c81d0e82aa7b4805a7248e56e74689d6 |
| Source note | uspto-grants-2004_08 |