Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851660Generated: October 26, 2026

Methyl iodide → 1,6,6-Trimethyl-piperidin-2-one

https://huagongshe.com/reaction/1851660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant6,6-Dimethylpiperidin-2-oneHCID 1714407—
Reactant3,3-Dimethylpiperidin-2-oneHCID 11240485—
SolventTetrahydrofuranHCID 8028—
Product1,6,6-Trimethyl-piperidin-2-oneHCID 8667301347%

Reaction Steps

To a solution of a 3 to 1 mixture of 3,3-dimethylpiperidin-2-one and 6,6-dimethylpiperidin-2-one (4.72 g, 37.1 mmol) in 60 ml of THF was added 60% sodium hydride suspension (1.93 g, 48.2 mmol). The grey reaction mixture was stirred at room temperature for 30 minutes. Then methyl iodide (3.02 ml, 48.2 mmol) was added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was quenched with water, and worked up with ethyl acetate/water. The orange oil was chromatographed over a prepacked 70 g silica column After elution with a 50% to 100% ethyl acetate in heptane gradient, the fractions containing the desired product were collected to yield 2.46 g (47%) of the title compound as a light yellow solid; and 0.91 g (17%) of isomeric 1,3,3-trimethyl-piperidin-2-one as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957213B2
Source datasetuspto-grants-2015_02
ORD IDord-9bc3fdde0f144ef6b26f352c0ca4a8ae
Source noteuspto-grants-2015_02