HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181908Generated: October 28, 2026
N-Fluorobenzenesulfonimide → tetraisopropyl difluoromethylenediphosphonate
https://huagongshe.com/reaction/1181908
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | tetraisopropyl difluoromethylenediphosphonate | HCID 11717839 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tetraisopropyl difluoromethylenediphosphonate | HCID 11717839 | — |
| Product | Tetrapropan-2-yl (fluoromethylene)bis(phosphonate) | HCID 12722940 | — |
Reaction Steps
To a stirred solution of tetraisopropyl difluoromethylenediphosphonate (4.5 g, 13.07 mmol) in anhydrous THF (20 mL) at −78° C. under argon were added sodium bis(trimethylsilyl)amide (1.0 M in THF, 28.7 mL) and N-fluorobenzenesulfonimide (9.89 g, 31.36 mmol). The reaction mixture was stirred at −78° C. for 1 h, quenched with saturated aqueous ammonium chloride (20 mL), warmed to room temperature, diluted with ether, washed with 10% aqueous sodium bicarbonate and then with brine, dried over sodium sulfate, and concentrated. Chromatography on silica gel with 5-30% ethyl acetate in hexanes gave 2.18 g of tetraisopropyl difluoromethylenediphosphonate and 0.32 g of tetraisopropyl monofluoromethylenediphosphonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07285658B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-95ebd247673540f6870ac8784c40f557 |
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| Source note | uspto-grants-2007_10 |
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