Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590636Generated: October 30, 2026

Epichlorohydrin → 5-(Oxiran-2-ylmethoxy)quinoline

https://huagongshe.com/reaction/1590636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium hydrideHCID 24758—
ReactantQuinolin-5-olHCID 135441757—
SolventDimethylformamideHCID 6228—
Product5-(Oxiran-2-ylmethoxy)quinolineHCID 1121789963.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

In 20 ml of dried DMF was dissolved 1 g of 5-hydroxyquinoline, and 0.28 g of sodium hydride (60% content) was then added thereto, followed by heating with stirring at 50° C. for 30 minutes. Afterward, 1.92 g of epichlorohydrin was further added to the reaction liquid and the latter was then heated with stirring at 90° C. for 3 hours, and the solvent was distilled off under reduced pressure. Water was then added to the residue, and the liquid was extracted with chloroform. The chloroform extract was then decolored and purified with active carbon, then was dried with anhydrous sodium sulfate, and was distilled off. The residue was then purified through a silica gel column chromatograph by the use of an effluent solvent of chloroform:methanol=100:1, so that 0.88 g of 5-(2,3-epoxypropoxy)quinoline was obtained in an oily state.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05204348
Source datasetuspto-grants-1993_04
ORD IDord-0bff4d315b99455ba7f5ca9c94208a15
Source noteuspto-grants-1993_04