HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → Phenol, 3-(2-hydroxyethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 86594026 | HCID 86594026 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenol, 3-(2-hydroxyethoxy)- | HCID 152273 | — |
Reaction Steps
To a solution of lithium aluminum hydride (455 mg, 12 mmol) in tetrahydrofuren was dropped ethyl [3-(acetyloxy)phenoxy]acetate (1.19 g, 5 mmol) in tetrahydrofuran (20 ml) at room temperature, and the mixture was stirred for 2 hours at room temperature. The reaction was quenched by 10% hydrochloric acid and the mixture was extracted with ethyl acetate. The organic layer was washed with water, 10% hydrochloric acid, an aqueous saturated sodium hydrogencarbonate solution and an aqueous saturated sodium chloride solution. The organic layer was dried over sodium sulfate. The solvent was removed under reduced pressure to give 3-(2-hydroxyethoxy)phenol (864 mg, quantitatively).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220773B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-ef28776f56a04eea9ba4e8638b4846c9 |
| Source note | uspto-grants-2007_05 |