Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Bromobenzophenone | HCID 70548 | — |
| Reactant | Tetraethyl [anthracene-9,10-diylbis(methylene)]bis(phosphonate) | HCID 16116648 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 73979916 | HCID 73979916 | — |
Reaction Steps
Under an inert atmosphere, 3-bromobenzophenone (3.917 g, 15 mmol), and 9,10-bis(diethylphosphonomethyl)anthracene (2.942 g, 6.17 mmol) are dissolved in tetrahydrofuran (40 g). At room temperature, tetrahydrofuran (16.38 g) solution of tert-butoxy potassium (2.070 g, 18.45 mmol) is added dropwise for 5 minutes, and successively stirred for 3.5 hours. The reaction mixture is charged into water (200 ml) and neutralized with 5% sulfuric acid. After neutralization, a hydrophobic solvent is added and the organic layer is partitioned. The organic layer is washed with water and dried over anhydrous sodium sulfate. The solvent is distilled off under reduced pressure, and the resultant raw product is purified by silica gel chromatography or recrystallization to give a desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875895B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-5ad8e55060ad406aadc904f7591c7960 |
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| Source note | uspto-grants-2005_04 |
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