Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | HCID 11163481 | HCID 11163481 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86641293 | HCID 86641293 | 39.2% |
Reaction Steps
To a solution of bisphosphonate 23 (8.02 g, 23.9 mmol) in DMF (24 mL) was added NaH (60% dispersion in mineral oil, 954 mg, 23.9 mmol) portionwise and the solution was stirred for 1.5 h at room temperature. A solution of p-nitrobenzyl bromide (7.75 g, 35.9 mmol) in THF (32 mL) was added and the mixture was stirred for 3 h at room temperature. It was then poured into a mixture of saturated aqueous NH4Cl solution and water and extracted with CH2Cl2 (3×). The combined organic layers were washed with saturated brine once, dried over MgSO4 and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel using a gradient of 0-50% EtOAc in CH2Cl2 as eluant to provide nitrobenzyl bisphosphonate 26 as a clear yellow oil (4.42 g, 9.38 mmol, 39%). 1H NMR (400 MHz, CDCl3) δ 2.73 (tt, J=23.8, 6.5 Hz, 1H), 3.37 (dt, J=16.4, 6.5 Hz, 2H), 4.51-4.61 (m, 8H), 5.21-5.25 (m, 4H), 5.29-5.35 (m, 4H), 5.83-5.93 (m, 4H), 7.44 (d, J=8.8 Hz, 2H), 8.14 (d, J=8.8 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08946144B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-d2d99db962944f0babb5cfba08c90e55 |
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| Source note | uspto-grants-2015_02 |
|---|