Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054824Generated: October 31, 2026

1-Benzyl-3-methyl-4-piperidone → 1-Benzyl-3,3-dimethylpiperidin-4-one

https://huagongshe.com/reaction/2054824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantSodium t-butoxideHCID 23676156—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-3,3-dimethylpiperidin-4-oneHCID 9794413—

Reaction Steps

To a solution of 1-benzyl-3-methyl-piperidin-4-one (7.0 g, 34 mmol) and Mel (2.4 mL) in THF (100 mL) was added NaOt-Bu (4.2 g, 44 mmol) at 0° C. The reaction was slowly allowed to warm to room temperature and stirred overnight. The aqueous layer was extracted with CH2Cl2. The organic extracts were combined, washed with brine and dried over MgSO4. The solution was filtered and concentrated in vacuo to give the crude product. Flash column chromatography (Hexane/EtOAc, gradient) of the residue gave 1-benzyl-3,3-dimethyl-piperidin-4-one, which was converted into 1-benzyl-3,3-dimethyl-piperidin-4-ylamine (2) using the same procedure as in Scheme 1-1. LCMS m/z: 220 (M+H)+. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329755B2
Source datasetuspto-grants-2008_02
ORD IDord-68fb17a82f1b4d6bab9bd4b3bbc47b8b
Source noteuspto-grants-2008_02