HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4,7-Dimethoxy-1,3-dihydro-2-benzofuran-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4,7-Dimethoxyphthalide | HCID 3703236 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4,7-Dimethoxy-1,3-dihydro-2-benzofuran-1-ol | HCID 15914472 | — |
Reaction Steps
To a solution of 6.19 g. of 4,7-dimethoxyphthalide in 500 ml. of methylene chloride which is cooled to -60° C. is added 48 ml. of diisobutylaluminum hydride in toluene and the mixture is stirred for one hour, 5 ml. of methanol is added and the solution is allowed to come to ambient temperature. The mixture is then treated with 600 ml. of chloroform and 300 ml. of sodium chloride solution and filtered. The organic layer is dried and the solvent removed to yield a white solid. This is washed with hexane to yield 4,7-dimethoxy-1,3-dihydro-1-isobenzofuranol having a melting point of 156°-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04032656 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-d3be507384cb49be88eda90e17ed577b |
| Source note | uspto-grants-1977_06 |