HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576957Generated: October 26, 2026
3-Quinolinecarboxaldehyde → (Quinolin-3-yl)methanol
https://huagongshe.com/reaction/576957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Quinolinecarboxaldehyde | HCID 83641 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (Quinolin-3-yl)methanol | HCID 12662983 | — |
Reaction Steps
In a 250 mL round bottom flask, quinoline-3-carbaldehyde (1.57 g, 10 mmol) was dissolved anhydrous ethanol (20 mL). The solution was cooled to 0° C. under nitrogen. NaBH4 (420 mg, 11 mmol) was added in one portion. The mixture was stirred at room temperature for 2 hours, and quenched by addition of water (3 mL). Na2SO4 (15 g) was added. After 10 minutes, the mixture was filtered. The filtrate was evaporated to provide quinolin-3-ylmethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09040538B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-5cb8498e4d874eee874d8ceafcc87088 |
|---|
| Source note | uspto-grants-2015_05 |
|---|