HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190919Generated: November 2, 2026
Diethyl Carbonate → 6-Fluoro-4-hydroxycoumarin
https://huagongshe.com/reaction/2190919
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | 2-Acetyl-4-fluorophenol | HCID 95992 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Fluoro-4-hydroxycoumarin | HCID 54691406 | 78% |
Reaction Steps
1-(5-Fluoro-2-hydroxy-phenyl)-ethanone (1.54 g, 10 mmol) and diethylcarbonate (2.42 mL, 20 mmol) were placed in a dry flask and dissolved in anhydrous tetrahydrofuran (30 mL.) The solution was then added drop-wise via cannula to a rapidly stirring solution of potassium tert-butoxide in tetrahydrofuran (1.0 M, 30 mL) The reaction was permitted to stir overnight (10 h) at room temperature under positive pressure of nitrogen. The crude reaction was concentrated under reduced pressure and partitioned between methyl tert-butyl ether and water. The layers were separated and the organic phase discarded. The aqueous phase was acidified to pH 5 and extracted three times with equal volumes of methylene chloride. The combined organic phases were dried over sodium sulfate and concentrated to give the title compound (1.4 g, 78% yield.) MS ESI(−) m/e: 179.16 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324405B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-f0fb5395ed3e4826ba67a0b53292924e |
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| Source note | uspto-grants-2012_12 |
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