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(2-Phenylquinolin-7-yl)methanol → 7-Methyl-2-phenylquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (2-Phenylquinolin-7-yl)methanol | HCID 22062823 | — |
| 反応物 | 2-Phenylquinoline-7-carbaldehyde | HCID 46835546 | — |
| 触媒 | Manganese dioxide | HCID 14801 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 7-Methyl-2-phenylquinoline | HCID 287715 | — |
反応手順
Additionally, 2-phenylquinoline-7-carbaldehyde could be prepared as follows: To a solution of (2-phenylquinolin-7-yl)methanol (75 mg, 0.319 mmol) in chloroform (1 mL) was added MnO2 (277 mg, 3.19 mmol). The mixture was stirred at rt for 20 h and filtered through a Celite pad. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel chromatography (1% MeOH in dichloromethane) to afford the title compound. 1H-NMR (CDCl3, 400 MHz) δ 7.50-7.59 (m, 3H), 7.95 (d, J=8.8 Hz, 1H), 8.04 (dd, J=2.4, 8.8 Hz, 2H), 8.19-8.22 (m, 2H), 8.31 (d, J=8.8 Hz, 1H), 8.69 (s, 1H), 10.26 (s, 1H). MS (ES+): m/z 234 [MH+]. HPLC: tR=3.59 min (OpenLynx, polar—5 min).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08653268B2 |
| 出典データセット | uspto-grants-2014_02 |
| ORD ID | ord-7266d67c0ae94cfa9fd667485130f3a1 |
| 出典メモ | uspto-grants-2014_02 |