HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618708Generated: October 28, 2026
Potassium Carbonate → 5,6-Difluorobenzofuran-2-carboxylic acid
https://huagongshe.com/reaction/618708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Reactant | 4,5-Difluoro-2-hydroxybenzaldehyde | HCID 15434553 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 5,6-Difluorobenzofuran-2-carboxylic acid | HCID 15434554 | 60.8% |
Reaction Steps
A mixture of 6.5 g (41.1 mmol) of 4,5-difluoro-2-hydroxybenzaldehyde, 10.4 ml (61.7 mmol) of diethyl bromo-malonate, 11.3 g (82.2 mmol) of potassium carbonate and 50 ml of ethyl methyl ketone was boiled at reflux for 3 hours while stirring, filtered and concentrated in a vacuum. The brown oil obtained was dissolved in 65 ml of ethanol, treated with 6.5 g of potassium hydroxide pellets and heated at reflux for one hour while stirring. The mixture was concentrated in a vacuum and the residue was treated with 65 ml of water and 65 ml of 3N sulfuric acid and heated at reflux over 30 minutes. Subsequently, the mixture was filtered and the residue was washed with water and triturated in 50 ml of hexane over 30 minutes. The solid was filtered off and dried. There were obtained 4.95 g (60%) of 5,6-difluorobenzofuran-2-carboxylic acid as a light yellow solid with m.p. 270°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05955495 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-dbf6806df07a401986d5a71c926d3cd0 |
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| Source note | uspto-grants-1999_09 |
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