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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238286Generated: October 30, 2026

1-Benzyl-4-piperidone → 1-Benzyl-4-methylpiperidin-4-ol

https://huagongshe.com/reaction/238286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-4-methylpiperidin-4-olHCID 10845913—

Reaction Steps

A solution of 1-benzyl-4-piperidone (26.5 mmol, 5 g) in THF (50 mL) was cooled to −15° C. and a solution of methyl magnesium bromide in ether (3 M, 22 mL) was added. The mixture was stirred for 0.5 hours then allowed to warm to room temperature. Saturated aqueous ammonium chloride (50 mL) was added and the products were extracted into ethyl acetate, dried over magnesium sulphate, filtered and the solvent removed by evaporation under vacuum to give the title compound as a pale yellow solid (5.0 g) that was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642621B2
Source datasetuspto-grants-2014_02
ORD IDord-7c4bdb5ed68c4c7db9fbbf0069da3577
Source noteuspto-grants-2014_02