HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557008Generated: October 29, 2026
1-Benzyl-4-piperidone → 1-Benzyl-4-methylpiperidin-4-ol
https://huagongshe.com/reaction/557008
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Benzyl-4-methylpiperidin-4-ol | HCID 10845913 | 83% |
Reaction Steps
A solution of 1-benzyl-4-piperidone (4.9 mL, 26.5 mmol) in anhydrous diethyl ether (50 mL) was cooled to −78° C. and treated with methyllithium (1.4 M, 21 mL, 29 mmol). This mixture was stirred for 2.5 hr at −78° C., then quenched with aqueous brine, and extracted with ethyl acetate (3×100 mL). The combined organics were dried over sodium sulfate and evaporated in vacuo. The residue was purified by silica gel chromatography (CH2Cl2→90:10:1 CH2Cl2/methanol/NH4OH) to yield 4.5 g (83%) of the title compound, ESI-MS m/z: 206 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058287B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-bd25c597926f4a05819ac14f7fe57de2 |
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| Source note | uspto-grants-2011_11 |
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