HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60299Generated: October 29, 2026
Sodium Hydroxide → (1,4-Dimethylpiperidin-4-yl)methanol
https://huagongshe.com/reaction/60299
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium aluminum hydride | HCID 28112 | — |
| Reactant | 1,4-Dimethylpiperidine-4-carboxylic acid hydrochloride | HCID 45595338 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1,4-Dimethylpiperidin-4-yl)methanol | HCID 20646825 | 73.3% |
Reaction Steps
To a stirred suspension of 1,4-dimethylpiperidine-4-carboxylic acid hydrogen chloride (1.00 g, 5.17 mmol) in tetrahydrofuran (18.9 mL) was added lithium tetrahydroaluminate (1.0N solution in tetrahydrofuran, 20.7 mL, 20.7 mmol) dropwise over 5 minutes. The reaction mixture was stirred at ambient temperature for 12 hours and then diluted with water (20 mL), basified to pH ˜12 by addition of sodium hydroxide pellets, and then diluted with diethyl ether (100 mL). The organic layer was separated, dried over sodium sulfate, filtered, and concentrated in vacuo to afford the title compound as a colorless oil (543 mg, 73%). 1H NMR (400 MHz, d6-DMSO) δ 4.44 (m, 1H), 3.12 (d, J=5.4, 2H), 2.50 (m, 2H), 2.39-2.31 (m, 2H), 2.13 (s, 3H), 2.12-2.09 (m, 1H), 1.42 (m, 2H), 1.16 (m, 2H), 0.82 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440976B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-70f093588dc54d528f1e39880060ca94 |
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| Source note | uspto-grants-2016_09 |
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