HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl benzofuran-7-carboxylate → Benzofuran-7-ylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl benzofuran-7-carboxylate | HCID 14229730 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzofuran-7-ylmethanol | HCID 18787422 | 91% |
Reaction Steps
A solution of methyl benzofuran-7-carboxylate (5.34 g, 30 mmol) was added to a suspension of LAH (2.31 g, 61 mmol) in THF and then heated to reflux for 30 min. The reaction was quenched with ethyl acetate and water. The mixture was made acidic with 12N HCl until all the precipitate dissolved. The ethyl acetate layer was separated, washed with water, dried with brine, and concentrated in vacuo to give a yellow oil (4.03 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856529 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-ef5c89c266084ae6b4feaf6821bd683a |
| Source note | uspto-grants-1999_01 |