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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302017Generated: October 29, 2026

Methanol → (2-Methylquinolin-4-yl)methanol

https://huagongshe.com/reaction/2302017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant2-MethylquinolineHCID 7060—
ReactantAmmonium SulfateHCID 6097028—
CatalystFerrous sulfate heptahydrateHCID 62662—
SolventWaterHCID 962—
Product(2-Methylquinolin-4-yl)methanolHCID 1014903327%

Reaction Steps

To a solution of quinaldine (75 g, 0.523 mol) in methanol (1100 mL) and water (550 mL) at room temperature was added sulfuric acid (28 mL, 0.523 mol) followed by iron(II) sulfate heptahydrate. Nitrogen was bubbled into the solution for 20 min and ammonium sulfate (177 g, 1.56 mol) was added. The resultant mixture was stirred in a water bath (20° C.) under nitrogen for 4 hours and quenched with 10% sodium hydroxide (pH=9-10). Methanol was removed by concentration in vacuo and the resulting aqueous solution was extracted with ethyl acetate three times. The combined organic phase was filtered through silica gel and washed with water and brine, dried (MgSO4) and concentrated. Crystallization from ethyl acetate gave 2-methyl-4-hydroxymethylquinoline (24.6 g, 27%) as a solid. MS(NH3-CI): (M+H)+=174.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06429213B1
Source datasetuspto-grants-2002_08
ORD IDord-8e5088eb23ab4431aca70eeafa44d9e8
Source noteuspto-grants-2002_08