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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349976Generated: October 26, 2026

Thionyl Chloride → 2-(5-Chloromethyl-2-pyridyloxymethyl)quinoline

https://huagongshe.com/reaction/349976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-(2-Quinolylmethoxy)-5-pyridylmethanolHCID 22413580—
Product2-(5-Chloromethyl-2-pyridyloxymethyl)quinolineHCID 2302495188%

Reaction Steps

A mixture of 6-(2-quinolylmethoxy)-3-pyridylmethanol (2.66 g) and thionyl chloride (10 ml) was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and saturated aqueous sodium bicarbonate solution was added to the residue, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography to obtain 2-(5-chloromethyl-2-pyridyloxymethyl)quinoline (2.50 g, yield 88%) as colorless crystals from the fraction eluted with ethyl acetate-hexane (1:1, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 118–119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-49dbf42a76a8459cab52bcdb01add345
Source noteuspto-grants-2007_02