HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzofuran-2-carboxylic acid → 1-Benzofuran-2-Ylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzofuran-2-carboxylic acid | HCID 10331 | — |
| Reactant | Diboron | HCID 6328200 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzofuran-2-Ylmethanol | HCID 2776263 | 78.5% |
Reaction Steps
1 Molar diborane in tetrahydrofuran (61.6 mL, 61.6 mmol) was added dropwise over 10 minutes to a stirred solution of benzofuran-2-carboxylic acid (5.00 g, 30.8 mmol) in tetrahydrofuran (50 mL) at 0° C. Stirring was continued at 0° C. for 30 minutes, then at room temperature for 18 hours. The reaction mixture was quenched carefully by slow addition of 1:1 tetrahydrofuran/water, and extracted with ether. The organic extracts were dried (MgSO4) and concentrated to afford 3.58 g (78%) of product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05084463 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-87334daa48d947ba843886d12d530459 |
| Source note | uspto-grants-1992_01 |