HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892432Generated: October 27, 2026
5,7-Difluoroquinoline-6-carbaldehyde → 1-(5,7-Difluoroquinolin-6-yl)ethanol
https://huagongshe.com/reaction/1892432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5,7-Difluoroquinoline-6-carbaldehyde | HCID 57917282 | — |
| Reactant | HCID 178461634 | HCID 178461634 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5,7-Difluoroquinolin-6-yl)ethanol | HCID 58190560 | 60.9% |
Reaction Steps
To a solution of 5,7-difluoroquinoline-6-carbaldehyde (5.0 g, 25.9 mmol) in THF (80 mL) was added ethylmagnesium iodide (3 M, 9.5 mL, 28.5 mmol) at −78° C. After stirring at −78° C. for 1 hour, the reaction was quenched with saturated NH4Cl and concentrated under reduced pressure. The residue was diluted with water, extracted with DCM three times. The organic layers were combined, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by chromatography (hexane/EtOAc) to give the title compound as a white solid (3.3 g, 58%). 1H-NMR (400 MHz, DMSO-d6) δ ppm 8.97 (dd, 1H), 8.47 (d, 1H), 7.66-7.58 (m, 2H), 5.54 (d, 1H), 5.29 (m, 1H), 1.56 (d, 3H). LCMS (method A): [MH]+=210, tR=4.71 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08507676B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-8a78545c110046d4aafe6e3d6b922007 |
|---|
| Source note | uspto-grants-2013_08 |
|---|