HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620210Generated: November 1, 2026
Sodium borohydride → (6-Ethoxy-2-(ethylamino)quinolin-3-yl)methanol
https://huagongshe.com/reaction/1620210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Ethoxy-2-(ethylamino)quinoline-3-carbaldehyde | HCID 86669819 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Ethoxy-2-(ethylamino)quinolin-3-yl)methanol | HCID 68182224 | 79% |
Reaction Steps
To a stirred solution of 6-ethoxy-2-(ethylamino)quinoline-3-carbaldehyde SLA 41034 (0.605 g, 2.48 mmol) in THF (50 mL) in a 250 mL round-bottomed flask equipped with a magnetic stirrer was added NaBH4 (0.094 g, 2.48 mmol) and the mixture was stirred overnight at RT then cooled in an ice bath before quenching by addition of a 1 N aq. HCl solution (40 mL). After stirring for 15 min at that temperature, the mixture was basified to pH=9 with a 2 N aq. NaOH solution. THF was then removed at 40° C. under vacuum and the solution was extracted with CH2Cl2 (200 mL), washed with brine (20 mL), dried over Na2SO4, filtered, and concentrated under vacuum to give (6-ethoxy-2-(ethylamino)quinolin-3-yl)methanol SLA 41040 as an orange solid (481 mg, 79% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08772316B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-e1171a1f4ca44c57a5433b8fff729372 |
|---|
| Source note | uspto-grants-2014_07 |
|---|