Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | Tetrapropan-2-yl (fluoromethylene)bis(phosphonate) | HCID 12722940 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methanefluorodiphosphonate | HCID 471181 | 269.5% |
Reaction Steps
To a stirred solution of tetraisopropyl fluoromethylenediphosphonate (320 mg, 0.88 mmol) in 1,2-dichloroethane (5 mL) was added dropwise trimethylsilyl bromide (0.70 mL, 5.28 mmol). The resulting solution was stirred at 40-42° C. for 24 h and 3 mL of anhydrous toluene was added. The mixture was concentrated to dryness, and coevaporated with toluene once. The residue was redissolved in DMF (3 mL)/water (2 mL) mixture and concentrated. The residue was mixed with DMF (2 mL) and tributylamine (0.42 mL, 1.76 mmol) and then concentrated to dryness. The residue was coevaporated with anhydrous DMF two times. The resulting residue was dried in a vacuum oven at 30° C. overnight to give a slightly yellow residue (460 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598230B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-001da96a64ec4180911e9d50ff0a49b6 |
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| Source note | uspto-grants-2009_10 |
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