HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259399Generated: October 25, 2026
Tetrahydrofuran → Diethyl 2-fluoro-2-phenylmalonate
https://huagongshe.com/reaction/2259399
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,4-Difluoro-1,4-diazoniabicyclo[2.2.2]octane bistriflate | HCID 15217965 | — |
| Reactant | C13H15NaO4 | HCID 178472663 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Diethyl 2-fluoro-2-phenylmalonate | HCID 4246642 | 65% |
Reaction Steps
A cold (-10° C.) solution of diethyl sodio(phenyl)-malonate in anhydrous tetrahydrofuran [prepared in conventional fashion from sodium hydride (2.5 mmol) and diethyl phenylmalonate (0.5 g, 2.1 mmol) in THF (15 cm3)] was added slowly to a cold (-10° C.) stirred solution of 1,4-difluoro-1,4-diazoniabicyclo[2.2.2]octane bistriflate (0.95 g, 2.12 mmol) in dry acetonitrile (50 cm3) under an atmosphere of nitrogen. The reaction mixture was allowed to warm to room temperature and then diluted with diethyl ether (100 cm3). The mixture was then washed with 0.5M oxalic acid (30 cm3), 10% aqueous potassium hydrogen carbonate (30 cm3), and saturated brine (30 cm3) (in that order), dried (MgSO4), filtered, and the filtrate evaporated under reduced pressure to provide diethyl fluoro(phenyl)-malonate (65% yield) with correct NMR parameters.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05473065 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-bff8bed15d45475c8f836dbd9ebfd39d |
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| Source note | uspto-grants-1995_12 |
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