HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3,4,4-Trimethylcyclohexan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Cyclohexen-1-one, 4,4-dimethyl- | HCID 136839 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3,4,4-Trimethylcyclohexan-1-one | HCID 13024934 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04147672 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-de584296ce414bccb4b8db53ce77af90 |
| Source note | uspto-grants-1979_04 |