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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Hydride | HCID 166653 | — |
| Reactant | N-methoxy-N-methyl-3,3-bis(diethoxyphosphinyl)propionamide | HCID 19689023 | — |
| Product | Tetraethyl 3-oxopentane-1,1-bisphosphonate | HCID 12499407 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05728650 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-513ee407692540e49f626f2d20b712d3 |
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| Source note | uspto-grants-1998_03 |
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