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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422595Generated: October 25, 2026

(2-Phenylquinolin-7-yl)methanol → 7-Methyl-2-phenylquinoline

https://huagongshe.com/reaction/422595

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Phenylquinolin-7-yl)methanolHCID 22062823—
Reactant2-Phenylquinoline-7-carbaldehydeHCID 46835546—
CatalystManganese dioxideHCID 14801—
SolventChloroformHCID 6212—
Product7-Methyl-2-phenylquinolineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101613B2
Source datasetuspto-grants-2012_01
ORD IDord-54600082035f4c49b17ef6c533b8b4a7
Source noteuspto-grants-2012_01