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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726450Generated: November 3, 2026

Methyl iodide → 1-Benzyl-3,3-dimethylpiperidin-4-one

https://huagongshe.com/reaction/1726450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
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 MeI (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. LC/MS m/z: 220 (M+H)+. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491827B2
Source datasetuspto-grants-2009_02
ORD IDord-d17a71e4d9f64891bc18b47f47159281
Source noteuspto-grants-2009_02