HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Phenylquinolin-7-yl)methanol → 7-Methyl-2-phenylquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Phenylquinolin-7-yl)methanol | HCID 22062823 | — |
| Reactant | 2-Phenylquinoline-7-carbaldehyde | HCID 46835546 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 7-Methyl-2-phenylquinoline | HCID 287715 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101613B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-54600082035f4c49b17ef6c533b8b4a7 |
| Source note | uspto-grants-2012_01 |