HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13593934, compound → 1-(2-Hydroxyethyl)cyclopentan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13593934 | HCID 13593934 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Hydroxyethyl)cyclopentan-1-ol | HCID 14101999 | 101.4% |
Reaction Steps
To a solution of tert-butyl 2-(1-hydroxycyclopentyl)acetate (0.5 g, 2.5 mmol) in THF (10 mL) was added lithium aluminium hydride (0.28 g, 7.5 mmol) portionwise at 0° C. The reaction was stirred at room temperature overnight. The mixture was partitioned between ethyl acetate and water. The combined organic layer was dried over sodium sulfate, filtered and concentrated to give a crude product which was purified by column chromatography eluting with petroleum ether/ethyl acetate (1:1) to give 1-(2-hydroxyethyl)cyclopentanol (0.33 g, 100%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359359B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-bb88191fbb334af3a0dfca3ee89ada6f |
| Source note | uspto-grants-2016_06 |