HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Methoxy-5,5-dimethylcyclohex-2-enone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4,4-Dimethyl-7-oxabicyclo[4.1.0]heptan-2-one | HCID 13553045 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methoxy-5,5-dimethylcyclohex-2-enone | HCID 55297986 | 68% |
Reaction Steps
A solution of 4,4-dimethyl-7-oxa-bicyclo[4.1.0]heptan-2-one (44.0 g, 0.31 mol) in methanol (150 mL) was added to a solution of 85% potassium hydroxide (20.7 g, 0.31 mol) in methanol (450 mL) at room temperature. The mixture was kept at this temperature for 20 hours and was then heated to reflux for 30 minutes. After cooling, the solution was diluted with water (1.2 L) and extracted with ethyl ether (350 mL×5). The organic extracts were collected, washed with brine, dried on Na2SO4 and evaporated under vacuum to remove most of the solvent. The crude material was purified by distillation to obtain pure the title compound (32.8 g, 68% yield) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541429B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-569f640ad5bc4509979fa057eae927af |
| Source note | uspto-grants-2013_09 |