HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3,5-Dimethoxy-1-benzofuran-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13682649 | HCID 13682649 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3,5-Dimethoxy-1-benzofuran-2-carboxylic acid | HCID 13682653 | 96% |
Reaction Steps
A mixture of 10.6 g (0.045 mole) of 3,5-dimethoxy-2 -benzofurancarboxylic acid, methyl ester in 80 ml of methanol is treated with 75 ml of 1.0 N aqueous sodium hydroxide solution. The new mixture is stirred at reflux for 45 minutes, cooled, and added to 750 g of ice/water. After extraction with dichloromethane, 3×300 ml) the aqueous layer is cooled in ice and acidified with glacial acetic acid to precipitate the crude product. The precipitate is filtered and washed with water to yield 9.6 g (88% crude yield) of 3,5-dimethoxy-2-benzofurancarboxylic acid. A sample recrystallized from ethyl acetate is analytically pure, mp 168° C.-dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04703053 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-ca4fddc7abee41a4801902f291214cbd |
| Source note | uspto-grants-1987_10 |