HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648219Generated: October 26, 2026
Sulfuric Acid → 5-Fluoro-1-benzofuran-2-carboxylic acid
https://huagongshe.com/reaction/648219
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Reactant | 5-Fluorosalicylaldehyde | HCID 2737328 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 5-Fluoro-1-benzofuran-2-carboxylic acid | HCID 10986872 | 19.4% |
Reaction Steps
5-Fluorosalicylaldehyde (4.4 g), diethylbromomalonate (11.3 g) and methyl ethyl ketone (35 ml) were stirred together. Anhydrous potassium carbonate (8.7 g) was added and the mixture was heated at reflux for 4 hours. Excess dilute sulphuric acid was added and the mixture was extracted with diethyl ether. The combined extracts were washed with water, dried and evaporated to leave an oil which was treated with 10% w/v ethanolic KOH (60 ml) and heated at reflux for 45 minutes. The solvent was evaporated and the residue treated with excess dilute sulphuric acid and heated briefly on a steam bath. After cooling the crude acid was filtered off. Recrystallisation from ethylacetate/ethanol gave a fawn coloured product (1.1 g), m.p. 261°-266° (decomp), I.R. νmax 1685 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04411908 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-56b195bf9af24788865628570bcd6060 |
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| Source note | uspto-grants-1983_10 |
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