HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-Benzofuran-3-yl-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | Methyl Benzofuran-3-acetate | HCID 10976279 | — |
| Product | 2-Benzofuran-3-yl-ethanol | HCID 68458256 | — |
Reaction Steps
A solution of benzofuran-3-yl-acetic acid methyl ester (4.0 g, 21 mmol) in 25 ml of ether was added dropwise at RT to a suspension of lithium alanate (1.61 g, 59.5 mmol) in 35 ml of ether, and stirring was then carried out for 30 minutes. Excess alanate was then hydrolysed with ethanol, the mixture was suction-filtered over Kieselguhr, and the solvent was removed in vacuo. The product was obtained in the form of a yellowish oil in a yield of 3.0 g (89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776848B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-59bad4e82581494b96c626227b667a12 |
| Source note | uspto-grants-2010_08 |