HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815809Generated: October 29, 2026
Sodium Hydroxide → 7-bromobenzofuran-5-carboxylic acid
https://huagongshe.com/reaction/1815809
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 22144801 | HCID 22144801 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-bromobenzofuran-5-carboxylic acid | HCID 22144751 | 82% |
Reaction Steps
A solution of 0.52 gm (2.03 mMol) 5-methoxycarbonyl-7-bromobenzofuran and 0.41 gm (10.13 mMol) sodium hydroxide in 4 mL ethanol was stirred at room temperature until all of the starting material had been consumed. The reaction mixture was concentrated under reduced pressure and the residue dissolved in water. This solution was then made basic by the addition of 1N sodium hydroxide and was extracted well with ethyl acetate. The remaining aqueous phase was made acidic (pH about 2) by treatment with potassium hydrogen sulfate and the resulting solid removed by filtration. The aqueous phase was extracted well with ethyl acetate and the organics were combined and concentrated under reduced pressure to provide 0.40 gm (82%) of 5-carboxy-7-bromobenzofuran as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06881733B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-d3f03d001fa9448e8b36a99372e56e74 |
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| Source note | uspto-grants-2005_04 |
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