HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 7-Methoxy-3-hydroxy-2,2-dimethylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 7-Methoxy-2,2-dimethyl-3-benzofuranone | HCID 14126647 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Methoxy-3-hydroxy-2,2-dimethylbenzofuran | HCID 14126648 | — |
Reaction Steps
An aqueous solution of sodium borohydride (8.2 g, 50 ml) is added to a stirred solution of the product obtained in Step 3. (41.8 g) in ethanol (1 l) and the mixture refluxed for 3 hours and evaporated in vacuo. The residue is taken up in water and toluene, the layers are separated and the organic phase washed, dried and evaporated in vacuo affording an oil which is dissolved in methylene chloride, dried, filtered and evaporated in vacuo. The residue is dissolved in ethyl acetate and chromatographed on silica gel affording the desired product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04722925 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-5b26df7fe2534bf0910c119f65b7be7d |
| Source note | uspto-grants-1988_02 |