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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654078Generated: November 1, 2026

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

https://huagongshe.com/reaction/1654078

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 numberUS05405843
Source datasetuspto-grants-1995_04
ORD IDord-870861b4b18744f29ac13f2cdb081cef
Source noteuspto-grants-1995_04