HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 6-Bromo-2,3-dihydro-1-benzofuran-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Bromo-1-benzofuran-3(2H)-one | HCID 44119520 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Bromo-2,3-dihydro-1-benzofuran-3-ol | HCID 68296741 | 92% |
Reaction Steps
To a solution of 6-bromo-benzofuran-3-one (10.5 g, 49.28 mmol) in methanol (100 ml) was added NaBH4 (2.37 g, 64.07 mmol) at 0° C. The reaction mixture was then stirred for 2 hours at room temperature. It was subsequently quenched with saturated ammonium chloride solution (50 ml) and extracted twice with ethyl acetate (2×50 ml). The combined organic phases were dried over Na2SO4 and evaporated under reduced pressure to give 9.75 g (92%) of the title compound as colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592426B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-8f7788a8c8d54cbf90a57bb66c3784ec |
| Source note | uspto-grants-2013_11 |