Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Bromo-2-ethoxy-1-methoxybenzene | HCID 21772690 | — |
| Reactant | HCID 25130165 | HCID 25130165 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69205124 | HCID 69205124 | 44.2% |
Reaction Steps
To a solution of 4-bromo-2-ethoxy-1-methoxy-benzene (0.67 g, 2.9 mmol) in THF (10 mL) was added a solution of n-butyllitium in hexane (1.1 mL, 2.5 N, 2.8 mmol) at −78° C. and kept for 20 min. To the mixture was added a solution of 3-fluoro-4,N-dimethoxy-N-methyl-benzamide (0.56 g, 2.6 mmol) in THF (4 mL) at −78° C. After 2 h, isopropanol (1 mL) and water (30 mL) was added to the mixture, and the cold bath was removed. The mixture was stirred at room temperature for 20 min. The mixture was extracted with ethyl acetate (2×50 mL). The combined organic layers was washed with HCl (0.5 N, 50 mL), sodium hydrogen carbonate (50 mL, sat), brine (50 mL) and dried over magnesium sulfate. Removal of solvent and chromatography (Silica Gel) gave (3-ethoxy-4-methoxy-phenyl) -(3-fluoro-4-methoxy-phenyl)-methanone (350 mg, 44% yield): 1H NMR (DMSO-d6) δ 1.49 (t, J=7 Hz, 3H, 2CH3), 3.96 (s, 3H, CH3), 3.98 (s, 3H, CH3), 4.16 (q, J=7 Hz, 2H, CH2), 6.90 (d, J=8 Hz, 1H, Ar), 7.02 (t, J=9 Hz, 1H, Ar), 7.35 (dd, J=2, 8 Hz, 1H, Ar), 7.41 (d, J=2 Hz, 1H, Ar), 7.55-7.62 (m, 2H, Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07470723B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-6c056e3b4e5746e6868975e23f2c2418 |
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| Source note | uspto-grants-2008_12 |
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