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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765546Generated: October 31, 2026

Allyl bromide → HCID 21107330, compound

https://huagongshe.com/reaction/1765546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant6-HydroxyquinolineHCID 11374—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductHCID 21107330HCID 2110733089.2%

Reaction Steps

To a suspension of sodium hydride (60%, 0.33 g, 8.3 mmol) in anhydrous N,N-dimethylformamide (30 ml) was added 6-hydroxyquinoline (1.0 g, 6.9 mmol) at room temperature. The reaction mixture was stirred for 1 hour, then allyl bromide (0.72 ml, 8.3 mmol) was added. The reaction mixture was allowed to stir for 1 hour at room temperature, quenched with water and extracted with methylene chloride. The organic layer was washed with water, dried over anhydrous sodium sulfate and filtered. The solvent was removed under vacuum. Chromatography (50% hexanes-ethyl acetate) afforded 1.14 g (89%) of 6-allyloxyquinoline as brown oil. MS ESI m/z 185 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07227023B2
Source datasetuspto-grants-2007_06
ORD IDord-274288f136b145bda3829e948eb73818
Source noteuspto-grants-2007_06