HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(benzofuran-3-yl)acetate → 2-(Benzofuran-3-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(benzofuran-3-yl)acetate | HCID 7537531 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Benzofuran-3-yl)ethanol | HCID 10953836 | — |
Reaction Steps
To a stirred suspension of LiAlH4 (200 mg, excess) in THF at 0° C., ethyl(-1-benzofuran-3-yl)acetate (1.02 g, 5 mmol) in THF (20 mL) was added slowly. After the addition, the reaction mixture was stirred at room temperature for 1 hr and quenched with saturated NH4Cl solution. The product was extracted with chloroform and washed well with water. It was dried over anhydrous MgSO4, filtered and concentrated. The product 2-(1-benzofuran-3-yl)ethanol obtained as a white oil was pure enough to be taken to next step without further purification. Yield: 800 mg (98%); (M+H): 163.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07276603B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-94884fb59d264a6bb5f25fae8ba84b0b |
| Source note | uspto-grants-2007_10 |