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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189203Generated: October 30, 2026

Toluene → 2-(4-Chloroquinolin-2-yl)phenol

https://huagongshe.com/reaction/2189203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant2,4-DichloroquinolineHCID 607503—
Reactant(2-Hydroxyphenyl)boronic acidHCID 2773454—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product2-(4-Chloroquinolin-2-yl)phenolHCID 13554705252.4%

Reaction Steps

2,4-Dichloroquinoline (0.500 g, 2.525 mmol), 2-hydroxyphenylboronic acid (0.332 g, 2.405 mmol), sodium carbonate (0.510 g, 4.810 mmol) and Pd(PPh3)4 (0.139 g, 120 mmol) were added to a degassed mixture of toluene (5 mL) and water (2 mL), and the mixture was heated for 15 hours. After cooling, water (100 mL) was added and the aqueous layer was extracted with ethyl acetate (2×100 mL). The organic layers were combined, washed with brine (50 mL), dried (MgSO4), and concentrated. The crude product was purified by silica gel chromatography (dichloromethane) to give the title compound (0.322 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324226B2
Source datasetuspto-grants-2012_12
ORD IDord-1e19368871854de286936ddf6f63ae6b
Source noteuspto-grants-2012_12