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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
Product1-Benzyl-4-methylpiperidin-4-olHCID 1084591383%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058287B2
Source datasetuspto-grants-2011_11
ORD IDord-bd25c597926f4a05819ac14f7fe57de2
Source noteuspto-grants-2011_11