Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluoro-2-(trifluoromethyl)benzaldehyde | HCID 522940 | — |
| Reactant | 6-Methoxy-3-methyl-2-phenyl-1-naphthol | HCID 68536388 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86616639 | HCID 86616639 | 90% |
Reaction Steps
Compound 7 (215 mg, 0.81 mmol, 1 equiv) was dissolved in DMF (5 mL) and cooled to 0° C. under N2. Sodium hydride, 60% dispersion (36 mg, 0.89 mmol, 1.1 equiv), followed by 4-fluoro-2-(trifluoromethyl)benzaldehyde (312 mg, 1.63 mmol, 2 equiv) were added and the entire reaction mixture was heated to 70° C. for 3 days. The mixture was then partitioned between EtOAc (50 mL) and H2O (50 mL). The organic layer was washed with saturated aqueous NaCl (100 mL), dried over Na2SO4, filtered and concentrated to dryness. The residue was purified by silica gel flash column chomatography (10% EtOAc in hexanes) to provide 20 (308 mg, 87%) as a clear oil. 1HNMR (400 MHz, DMSO-d6): δ 10.01 (s, 1H), 7.89 (d, J=8.8 Hz, 1H), 7.78 (s, 1H), 7.60 (d, J=9.1 Hz, 1H), 7.39 (d, J=2.4 Hz, 1H), 7.32-7.10 (m, 7H), 6.95 (dd, J=8.6, 2.4 Hz, 1H), 3.88 (s, 3H), 2.20 (s, 3H). MS m/z 473.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07649093B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-958795c2b1374783bec9c4b14a3fdbe0 |
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| Source note | uspto-grants-2010_01 |
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