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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25888Generated: October 25, 2026

Methyl iodide → 3,4,4-Trimethylcyclohexan-1-one

https://huagongshe.com/reaction/25888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Cyclohexen-1-one, 4,4-dimethyl-HCID 136839—
ReactantMagnesiumHCID 5462224—
CatalystCuprous chlorideHCID 62652—
SolventDiethyl EtherHCID 3283—
Product3,4,4-Trimethylcyclohexan-1-oneHCID 1302493463%

Reaction Steps

109 g of CuCl were added in small portions to a Grignard solution prepared from 26.4 g of magnesium turnings and 156.2 g of methyliodide in 200 ml diethylether under a nitrogen atmosphere. To the reaction mixture there were then added 124 g of 4,4-dimethyl-cyclohex-2-en-1-one in ether solution and the whole was refluxed for 2 h. The mixture was then hydrolysed with a saturated aqueous solution of ammonium chloride and subjected to the usual treatments to afford on distillation 88 g (63% yield) of 3,4,4-trimethyl-cyclohexanone;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04147672
Source datasetuspto-grants-1979_04
ORD IDord-de584296ce414bccb4b8db53ce77af90
Source noteuspto-grants-1979_04