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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970Generated: October 25, 2026

Tetrahydrofuran → Tetraethyl 3-oxopentane-1,1-bisphosphonate

https://huagongshe.com/reaction/1970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHydrideHCID 166653—
ReactantN-methoxy-N-methyl-3,3-bis(diethoxyphosphinyl)propionamideHCID 19689023—
ProductTetraethyl 3-oxopentane-1,1-bisphosphonateHCID 1249940754%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of N-methoxy-N-methyl-3,3-bis(diethoxyphosphinyl)propionamide (1.00 g, 2.6 mmol) in THF (5 ml) was slowly added to a slurry of 80% sodium hydride (80 mg, 2.7 mmol) in THF (10 ml) at 0° C. Stirring was continued until all of the hydride was consumed (~20 minutes). The solution was cooled to -78° C. and ethylmagnesium bromide (1.0 ml of a 3.0M solution in diethyl ether, 3.0 mmol) was added. After the addition, the reaction mixture was warmed to 0° C. and stirred for one hour. The reaction was quenched by pouring slowly into a well-stirred ice-cold mixture of ethanol (40 ml) and concentrated HCl (5 ml). The solvents were removed in vacuo, the residue was taken up in brine (20 ml) and extracted with dichloromethane (4×20 ml). The combined extracts were dried (Na2SO4), concentrated in vacuo, and the resulting oil was purified by flash chromatography on silica gel eluting with 10% i-propanol in ethyl acetate to give the title compound (0.50 g, 54%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728650
Source datasetuspto-grants-1998_03
ORD IDord-513ee407692540e49f626f2d20b712d3
Source noteuspto-grants-1998_03