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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869795Generated: October 26, 2026

Phenol → 6-(Benzyloxy)-2-phenoxyquinoline

https://huagongshe.com/reaction/1869795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantSodium HydroxideHCID 14798—
ReactantTetrabutylammoniumHCID 16028—
Reactant6-(Benzyloxy)-2-chloroquinolineHCID 11219424—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product6-(Benzyloxy)-2-phenoxyquinolineHCID 11771782—

Reaction Steps

To a 50% (w/w) NaOH solution (10.2 ml) is added phenol (0.697 g). After 50 minutes at room temperature, toluene (10.21 ml) and 6-(benzyloxy)-2-chloroquinoline 12 (2 g) and tetrabutyl ammonium (2.062 g) are added. The solution is stirred under argon at reflux for 24 h. Water (5 ml) is added and the solution is extracted with toluene (3×10 ml). The organic phases are dried over MgSO4 and evaporated under vacuum. The residue is purified by silica gel chromatography using AcOEt/cyclohexane 20/80 as eluent. The obtained solid is dissolved in AcOEt and pentane is added; 6-(benzyloxy)-2-phenoxyquinoline 13 precipitates as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638630B2
Source datasetuspto-grants-2009_12
ORD IDord-9fcfcab1d533481586d817cb4514b5a2
Source noteuspto-grants-2009_12