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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12032Generated: October 26, 2026

Methyl iodide → 2,2-Dimethylcyclohexan-1-one

https://huagongshe.com/reaction/12032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylboraneHCID 7357—
Reactant2-MethylcyclohexanoneHCID 11419—
ReactantPotassium hydrideHCID 82127—
SolventTetrahydrofuranHCID 8028—
Product2,2-Dimethylcyclohexan-1-oneHCID 136929—

Reaction Steps

A suspension of potassium hydride (5.5 mmol) and 2-methylcyclohexanone (5 mmol) in dry tetrahydrofuran (10 ml) is stirred for 30 mins at room temperature. Triethylborane (6.25 mmol) is slowly added dropwise and the mixture is stirred for 16 hours at room temperature. After addition of methyl iodide stirring is continued for another 8 hours, the reaction is then quenched with saturated aqueous ammonium chloride solution and twice extracted with diethyl ether. The combined organic phases are dried over sodium sulphate and concentrated to dryness in a vacuum and produce the title compound, which can be reacted without [without] purification (JACS 1985, 107, 19, 5391-5396).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727979B2
Source datasetuspto-grants-2010_06
ORD IDord-86101b2e7f9945179d50d853ef03d403
Source noteuspto-grants-2010_06