HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60829Generated: October 29, 2026
Aluminium lithium hydride → 5,5-Diethoxy-2-piperidinemethanol
https://huagongshe.com/reaction/60829
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 5,5-diethoxypiperidine-2-carboxylate | HCID 89739186 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,5-Diethoxy-2-piperidinemethanol | HCID 89739172 | 95% |
Reaction Steps
A suspension of LAH (0.47 g, 12.25 mmol) in anhydrous THF (5 mL) was added a solution of ethyl 5,5-diethoxypiperidine-2-carboxylate (0.6 g, 2.45 mmol) in anhydrous THF (5 mL) dropwise at rt. The resulting mixture was refluxed at 70° C. for overnight. The reaction mixture was cooled down to 0° C. and quenched sequentially with water (0.47 g), 15% NaOH (0.47 g) and water (1.41 g). The resulting suspension was stirred at rt for 1 h and filtered. The filtrate was concentrated in vacuo to give desired rac-(5,5-diethoxypiperidin-2-yl)methanol in 95% yield as colorless oil. 1H NMR (CDCl3, 400 MHz) δ 3.54-3.32 (m, 6H), 3.11-3.04 (m, 1H), 2.56-2.46 (m, 2H), 2.05-2.00 (m, 1H), 1.52-1.23 (m, 3H), 1.15-1.07 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09440982B2 |
|---|
| Source dataset | uspto-grants-2016_09 |
|---|
| ORD ID | ord-d0c96c15ec804e5a936bfdb6cea39d58 |
|---|
| Source note | uspto-grants-2016_09 |
|---|