HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203659Generated: November 2, 2026
2-Acetylpyridine → alpha-Methyl-2-pyridinemethanol
https://huagongshe.com/reaction/2203659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Acetylpyridine | HCID 14286 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | alpha-Methyl-2-pyridinemethanol | HCID 86784 | 92% |
Reaction Steps
To an ice-cooled solution of 1-(pyridin-2-yl)ethanone (11 g, 91 mmol) in methanol (120 mL) was slowly added sodium borohydride (8.58 g, 227 mmol). Upon complete addition, the mixture was warmed to 25° C. After 16 h, the reaction was diluted with water (100 mL), and the mixture was concentrated in vacuo. The resulting aqueous solution was extracted with ethyl acetate (3×100 mL). The combined organic extracted were washed with saturated aqueous sodium chloride (2×50 mL), dried over anhydrous sodium sulfate, filtered, and concentrated. Purification by flash column chromatography (10→30% ethyl acetate in petroleum ether) afforded 1-(pyridin-2-yl)ethanol (10.3 g, 92% yield). 1H NMR (400 MHz, Chloroform-d) δ 8.54 (d, J=4.8 Hz, 1 H), 7.72-7.68 (m, 1 H), 7.30 (d, J=8.0 Hz, 1 H), 7.22-7.20 (m, 1 H), 4.93-4.88 (m, 1 H), 4.39 (br s, 1 H), 1.52 (d, J=6.4 Hz, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09365583B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-81ea466aaefa488096734cd601ffd991 |
|---|
| Source note | uspto-grants-2016_06 |
|---|