HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Methoxy-1-benzofuran-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-methoxybenzofuran-2-carboxylate | HCID 22729192 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Methanol tetrahydrofuran water | HCID 21892291 | — |
| Product | 4-Methoxy-1-benzofuran-2-carboxylic acid | HCID 22728982 | 96% |
Reaction Steps
To a suspension of methyl 4-methoxy-benzofuran-2-ylcarboxylate (206 mg, 1.0 mmol) in THF/methanol/water (6 ml, 1/1/1) was added 2M aqueous NaOH (1.0 ml) and refluxed until saponification was completed (˜3 h). The reaction mixture was acidified with 1M aqueous HCl (10 ml) and diluted with ethyl acetate (30 ml). The separated organic layer was washed with 1M aqueous HCl (30 ml), brine (30 ml), dried over sodium sulfate, and concentrated in vacuo to provide 4-methoxy-benzofuran-2-ylcarboxylic acid as a white solid (189 mg, 0.96 mmol), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368572B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-feac74690d5846dd8efa2c06e067b722 |
| Source note | uspto-grants-2008_05 |