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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216752Generated: October 26, 2026

8-Methyl-2-o-tolylquinoline-3-carbaldehyde → 1-(8-Methyl-2-o-tolylquinolin-3-yl)ethanol

https://huagongshe.com/reaction/216752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Methyl-2-o-tolylquinoline-3-carbaldehydeHCID 57707895—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product1-(8-Methyl-2-o-tolylquinolin-3-yl)ethanolHCID 57707813—

Reaction Steps

Prepared according to Procedure K. To a mixture of 8-methyl-2-o-tolylquinoline-3-carbaldehyde (434 mg, 1.7 mmol) in THF (6 mL) at 0° C. was added dropwise a solution of MeMgCl (3M, 2 eq, 1.1 mL) and the reaction was stirred over night before quenched with NH4Cl saturated solution. The mixture was extracted with EtOAc (2×10 mL) and the combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: EtOAc/hexane, 1/1) to provide 1-(8-methyl-2-o-tolylquinolin-3-yl)ethanol as a white solid. 1H-NMR (CDCl3) δ 8.34 (s, 1H), 7.66 (d, J=8.2 Hz, 1H), 7.48 (d, J=6.7 Hz, 1H), 7.39 (t, J=7.8 Hz, 1H), 7.19-7.27 (m, 4H), 2.69 (s, 3H), 2.08 (s, 3H), 1.30 (m, 3H). Mass Spectrum (ESI) m/e=278 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193199B2
Source datasetuspto-grants-2012_06
ORD IDord-42f3119a0a294b36803248c316eefb2d
Source noteuspto-grants-2012_06