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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025535Generated: October 27, 2026

5-Chloro-8-hydroxyquinoline → HCID 15274186, compound

https://huagongshe.com/reaction/1025535

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-8-hydroxyquinolineHCID 2817—
ReactantAllyl bromideHCID 7841—
ReactantSodium HydroxideHCID 14798—
CatalystTetrabutylammonium BromideHCID 74236—
SolventBenzeneHCID 241—
ProductHCID 15274186HCID 1527418677.4%

Reaction Steps

A solution of 5-chloro-8-hydroxyquinoline (1 mmol, 180 mg) in aqueous NaOH (0.25 M, 8 mL; 2 mmol) containing tetrabutylammonium bromide as the phase-transfer catalyst (0.1 mmol, 33 mg) was stirred for 30 min., and allyl bromide (1 mmol, 85 μL) and benzene (8 mL) were added and the reaction mixture was stirred vigorously at 50° C. for 14 h. The reaction mixture was partitioned between water (15 mL) and EtOAc (15 mL) after cooling to room temperature and the extraction was repeated twice. The organic layers were combined and washed with 1 M NaOH solution (15 mL) and concentrated. The crude product was purified by flash-column chromatography over silica gel using 1:2 hexanes-ether as eluent to afford quinoline 3a as a light-brown solid (170 mg, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729097B2
Source datasetuspto-grants-2014_05
ORD IDord-0d67a59054c34cdebc98c2d61b42cd28
Source noteuspto-grants-2014_05