HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(5,5-Dimethylcyclohex-1-en-1-yl)ethan-1-one → HCID 20569421, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(5,5-Dimethylcyclohex-1-en-1-yl)ethan-1-one | HCID 12668519 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20569421 | HCID 20569421 | 85% |
Reaction Steps
A solution of 1-(5′,5′-dimethylcyclohex-1′-enyl)ethanone (13.1 g, 85.8 mmol) in Et2O (50 ml) was added dropwise with stirring within 50 min. to a suspension of LAH (895 mg, 23.6 mmol) in Et2O (150 ml). The reaction mixture was refluxed for 1 h prior to quenching at 0° C. by careful addition of water (50 ml) followed by 5 N aq. HCl (50 ml). The organic layer was separated and the aqueous one extracted with Et2O. The combined ethereal solutions were washed with water and brine, dried (Na2SO4), and concentrated in a rotary evaporator. Silica-gel FC (pentane/Et2O, 9:1, Rf=0.14) of the resulting residue (14.7 g) gave 11.2 g (85%) of 1-(5′,5′-dimethylcyclohex-1′-enyl)ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07393822B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-aaf271fcf2e345e0aff63f8e9b08bf0c |
| Source note | uspto-grants-2008_07 |