HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260569Generated: October 31, 2026
P,P,P′,P′-Tetraethyl P,P′-ethylidenebis[phosphonate] → HCID 13612965, compound
https://huagongshe.com/reaction/260569
Participants
| Role | Name | HCID | Charge |
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| Reactant | P,P,P′,P′-Tetraethyl P,P′-ethylidenebis[phosphonate] | HCID 11077490 | — |
| Reactant | HCID 21478260 | HCID 21478260 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13612965 | HCID 13612965 | — |
Reaction Steps
A solution of 13.29 g (40 mmol) of tetraethyl ethane-1,1-diphosphonate in 120 ml of dry tetrahydrofuran was cooled to -78° C. in an argon atmosphere followed by the addition of 24.24 ml (40 mmol) of a n-butyllithium hexane solution (1.65 mmol/ml) and stirring for 30 minutes. After adding a solution of 7.63 g (40 mmol) of 4-methylthiobenzenesulfenyl chloride in 50 ml of dry tetrahydrofuran to this mixture, the reaction mixture was allowed to warm up to room temperature followed by stirring for 3 hours. After pouring the resulting mixture into icewater, the mixture was extracted with ethyl acetate (3×150 ml). The solvent was distilled off under reduced pressure after the combined organic layer was washed with water and saturated brine and dried over anhydrous magnesium sulfate. A mixture of tetraethyl 1-methylthiophenyl)thio]ethane-1,1-diphosphonate and tetraethyl 1-chloroethane-1,1-diphosphonate was obtained as the residue. This mixture was then carefully purified with column chromatography (developing solvent: ethanol: ethyl acetate=5:95) to obtain 7.12 g of the target compound in the form of a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05527940 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-be1d75ef418047f791d67711a119755c |
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| Source note | uspto-grants-1996_06 |
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