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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181908Generated: October 28, 2026

N-Fluorobenzenesulfonimide → tetraisopropyl difluoromethylenediphosphonate

https://huagongshe.com/reaction/1181908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactanttetraisopropyl difluoromethylenediphosphonateHCID 11717839—
SolventTetrahydrofuranHCID 8028—
Producttetraisopropyl difluoromethylenediphosphonateHCID 11717839—
ProductTetrapropan-2-yl (fluoromethylene)bis(phosphonate)HCID 12722940—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285658B2
Source datasetuspto-grants-2007_10
ORD IDord-95ebd247673540f6870ac8784c40f557
Source noteuspto-grants-2007_10