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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495423Generated: October 31, 2026

8-Hydroxyquinoline → 8-allyloxyquinoline

https://huagongshe.com/reaction/495423

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-HydroxyquinolineHCID 1923—
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product8-allyloxyquinolineHCID 46135972%

Reaction Steps

To a suspension of sodium hydride (60% oil dispersion, 3.0 g, 75 mmol) in DMF (100 mL) at 0° C. under argon, was added a solution of 8-hydroxyquinoline (9.2 g, 64 mmol) in DMF (20 mL) dropwise. The mixture was allowed to stir for 0.5 h, then allyl bromide (6.6 mL, 77 mmol) was added dropwise. The mixture was stirred at room temperature for 20 h, then was poured into ice/water (400 mL) and extracted with ether (3×300 mL). Combined organic extracts were washed with water (500 mL) and evaporated in vacuo. The crude residue was purified by silica gel chromatography (ethyl acetate in hexane 25%-75% gradient) to give 8-allyloxyquinoline (8.5 g, 72%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939871B2
Source datasetuspto-grants-2005_09
ORD IDord-ba6fc45f0ca14819b446dac12332dc5a
Source noteuspto-grants-2005_09