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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569603Generated: October 31, 2026

Sodium hydride → Tetraethyl (phenoxymethylene)-bisphosphonate

https://huagongshe.com/reaction/569603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDichloromethyl phenyl etherHCID 319898—
ReactantDiethylphosphiteHCID 3780918—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductTetraethyl (phenoxymethylene)-bisphosphonateHCID 54483224—

Reaction Conditions

Temperature0 °C

Reaction Steps

Diethylphosphite (20.6 ml) was added dropwise at 20° C. to a stirred suspension of 55% sodium hydride (6.24 g) in dimethylformamide (90 ml). After stirring for a further 15 minutes, the mixture was cooled to 0° C., and dichloromethyl phenyl ether (9.27 g) was added dropwise. Stirring was continued overnight at 45° C., and the mixture was cooled in ice, diluted with water, neutralized and extracted with ethyl acetate. The organic phase was washed repeatedly with water, dried and evaporated in vacuo to yield an oil which was purified by chromatography on silica gel. Eluent: ether-acetone 85:15. The pure title compound was obtained as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04732998
Source datasetuspto-grants-1988_03
ORD IDord-ddd21daf02a64cb48d14aab9fefdbfa2
Source noteuspto-grants-1988_03