HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590636Generated: October 30, 2026
Epichlorohydrin → 5-(Oxiran-2-ylmethoxy)quinoline
https://huagongshe.com/reaction/1590636
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Quinolin-5-ol | HCID 135441757 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(Oxiran-2-ylmethoxy)quinoline | HCID 11217899 | 63.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05204348 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-0bff4d315b99455ba7f5ca9c94208a15 |
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| Source note | uspto-grants-1993_04 |
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