HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Quinolinemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Quinolinecarboxaldehyde | HCID 79619 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Quinolinemethanol | HCID 73196 | 88% |
Reaction Steps
A solution of 3.0 g of quinoline-2-carboxaldehyde in 100 ml of ethanol was treated with 750 mg of sodium borohydride and stirred at ambient temperature for 15 min. The resulting solution was neutralized with 1N HCl, concentrated in vacuo, and extracted three times with ethyl acetate. The combined organic layers were dried over Na2SO4 and concentrated to provide 2.65 g (88%) of the crude desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616714 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-1ab4b932eb7a44b190073a611411ade3 |
| Source note | uspto-grants-1997_04 |