HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2,2,5,5-Tetramethylcyclopentan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,2,5,5,-Tetramethylcyclopentanone | HCID 138287 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2,5,5-Tetramethylcyclopentan-1-ol | HCID 551696 | 81.5% |
Reaction Steps
To a magnetically stirred solution of 10 g (0.071 mol) 2,2,5,5-tetramethylcyclopentanone in 75 ml of dry tetrahydrofuran at 0° C. under argon is added 2.69 g (0.071 mol) of lithium aluminum hydride. When the reduction was complete, ethyl acetate was introduced dropwise to destroy unreacted lithium aluminum hydride. 25 mls of water is then added, followed by 300 mls of diethyl ether. The organic phase is washed with 100 mls of water, and dried over MgSO4. Filtration followed by evaporation afforded 8.23 g of 2,2,5,5-tetramethylcyclopentanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788332 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-7813728b7d8946549a74a52d82135583 |
| Source note | uspto-grants-1988_11 |