Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57799945 | HCID 57799945 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57799915 | HCID 57799915 | 77.2% |
Reaction Steps
To a stirred solution of crude 2-((dimethylamino)methyl)-3-(3-fluoro-2-methylphenyl)-1,5-bis(3-methoxyphenyl)-4-methylenepentane-1,5-dione (91 g, 186 mmol) in acetonitrile (769 mL) was added diisopropylethylamine (65 mL, 376 mmol) followed by iodomethane (140 mL, 2.24 mol). The mixture was stirred at room temperature for 16 h. To this mixture was added 2 M KOH (307 mL, 614 mmol), and the temperature was raised to 75° C. for 16 h. The mixture was partitioned between dichloromethane and water. The layers were separated and the aqueous phase extracted with 500 mL dichloromethane. The combined organic layers were dried over MgSO4, filtered, and evaporated to dryness. The residue was treated with 350 mL ether, isolated by filtration, and washed with 2×100 mL of ether. The ether layers were concentrated in vacuum to give 3-(3-fluoro-2-methylphenyl)-1,5-bis(3-methoxyphenyl)-2,4-dimethylenepentane-1,5-dione (63.8 g, 77% yield), (characterized by LCMS and 1H NMR). LRMS (M+H+) m/z=445.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572814B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-499f344b7fec4c908a5f68ec05031040 |
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| Source note | uspto-grants-2009_08 |
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