HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(5-Fluoropyridin-2-yl)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-(5-Fluoropyridin-2-yl)ethan-1-one | HCID 59868831 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(5-Fluoropyridin-2-yl)ethan-1-ol | HCID 59186883 | 87.3% |
Reaction Steps
1-(5-Fluoropyridin-2-yl)ethanone (Method 1; 11.3 g, (75% pure), 60.9 mmol) in MeOH was added sodium boronhydride (2.30 g, 60.9 mmol) potion wise at 0° C. After adding, the reaction was warmed to room temperature and stirred at room temperature for 1 hour. Water (10 ml) was added and the solution was extracted with ether (2×50 ml). The combined organic layers were dried over sodium sulfate. After removal of solvent, the resulted residue was purified by column chromatography (ether) to give the title compound as a clear oil (7.5 g, 87%). 1H NMR (400 MHz) 8.46 (d, J=3.2 Hz, 1H), 7.69 (ddd, J=3.2, 3.2 and 3.2 Hz, 1H), 7.55 (m, 1H), 5.44 (d, J=4.4 Hz, 111), 4.73 (m, 1H), 1.34 (d, J=6.4 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114989B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-f81a88fb3f8549e5a40c9971cc6b617a |
| Source note | uspto-grants-2012_02 |