HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3-(1-Methoxy-1-Phenylethyl)-4-Phenyl-8-(Trifluoromethyl)Quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Phenyl-1-[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]ethanol | HCID 11349896 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(1-Methoxy-1-Phenylethyl)-4-Phenyl-8-(Trifluoromethyl)Quinoline | HCID 66913189 | — |
Reaction Steps
1-Phenyl-1-[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]ethanol (Example 39, 0.096 g, 0.243 mmol) was taken into DMF (3 mL) then NaH (0.020 g, 0.487 mmol) was added and stirred for 20 minutes. Lastly, iodomethane (0.08 mL, 1.22 mmol) was added and stirring was continued for 30 minutes. The reaction was quenched with water and extracted with ether. The combined organics were dried over magnesium sulfate and concentrated. The resulting material was purified via column chromatography using 5% ethyl acetate in hexane as the eluent. MS (ESI) m/z 408 ([M+H]+); 1H NMR (CDCl3) δ 9.59 (s, 1H), 8.01 (d, J=6.8 Hz, 1H), 7.31 (m, 3H), 7.12 (m, 5H), 7.0 (m, 2H), 6.74 (dd, J=7.5 and 1.2 Hz, 1H), 6.63 (dd, J=7.7 and 1.3 Hz, 1H), 3.06 (s, 3H), 1.8 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576215B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-4b8eeb439e5949cb8c8515e2b8b70e0c |
| Source note | uspto-grants-2009_08 |