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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25888Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/25888

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktAmmonium ChlorideHCID 25517—
Edukt2-Cyclohexen-1-one, 4,4-dimethyl-HCID 136839—
EduktMagnesiumHCID 5462224—
KatalysatorCuprous chlorideHCID 62652—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3,4,4-Trimethylcyclohexan-1-oneHCID 1302493463%

Reaktionsschritte

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;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04147672
Quelldatensatzuspto-grants-1979_04
ORD IDord-de584296ce414bccb4b8db53ce77af90
Quellennotizuspto-grants-1979_04