HuagongsheHuagongshe Chemistry Print Report · For research reference only
(6-Hydroxy-1-benzofuran-3-yl)acetate → (S)-Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (6-Hydroxy-1-benzofuran-3-yl)acetate | HCID 2110914 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate | HCID 53393313 | — |
Reaction Steps
To a mixture of (1,5-cyclooctadiene)rhodium trifluoromethanesulfonate (656 mg) and (S,S)-Et-FerroTANE (620 mg) was added methanol (200 mL) sufficiently substituted by argon gas, and the mixture was stirred at room temperature 15 min. To a mixture of (6-hydroxy-1-benzofuran-3-yl)acetate (26.1 g) and sodium methoxide (3.8 g) was added methanol (500 mL) sufficiently substituted by argon gas. The methanol solution prepared earlier was added thereto, and the mixture was stirred at room temperature for 2 hr under 0.7 MPa hydrogen atmosphere. The reaction mixture was quantified by HPLC. As a result, the enantiomeric excess was 90.8%, the yield was quantitative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732626B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-d7feccbbbb364cd2b29ad19b7d46332a |
| Source note | uspto-grants-2010_06 |