Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | CLODRONIC ACID,TETRAETHYL ESTER | HCID 2785333 | — |
| Reactant | HCID 131718818 | HCID 131718818 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15786045 | HCID 15786045 | — |
Reaction Steps
5.0 g (0.014 moles) of tetraethyl (dichloromethylene)bisphosphonate and 6.7 g (0.045 moles) of NaI are dissolved in 50 ml of anhydrous CH3CN and while stirring 12.2 g (0.112 moles) of trimethylsilyl chloride are added. After the addition stirring is continued at room temperature, protected from moisture, for appr. 4 days and is evaporated under a vacuum. To the mixture obtained as a residue (contains as the major component monoethyl tris(trimethylsilyl) (dichloromethylene)bisphosphonate) 10 ml of water are added and the mixture is made alkaline with a 10% NaOH solution. The mixture is diluted with 50 ml of CH3OH and is left standing at +4° C. for 2 h and is filtered (the precipitate is (dichloromethylene)bisphosphonic acid sodium salt). To the filtrate 25 ml of ethanol are added and it is left standing for 1 day at +4° C. and is filtered. The filtrate is evaporated under a vacuum and the residue is washed with acetone and filtered. The precipitate is dried to constant weight whereby appr. 2.0 g (50% of the theor.) of colourless crystalline (dichloromethylene)bisphosphonic acid monoethyl ester trisodium salt are obtained (31P-NMR (D2O): δ 6 11.86 (P), 9.40 (P') 2JPP =15.4 Hz) at a concentration of >90% and wherefrom the corresponding acid may be liberated with acid treatment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05376649 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-75de7d753d9f45a2b55e56bc1fc861f8 |
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| Source note | uspto-grants-1994_12 |
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