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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277382Generated: October 31, 2026

4-Nitrophenol → 7-(Benzyloxy)-4-(4-nitrophenoxy)quinoline

https://huagongshe.com/reaction/2277382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantDichloromethaneHCID 6344—
ReactantDiisopropylethylamineHCID 81531—
Reactant7-(Benzyloxy)-4-chloroquinolineHCID 22030657—
SolventTolueneHCID 1140—
Product7-(Benzyloxy)-4-(4-nitrophenoxy)quinolineHCID 6819394295.7%

Reaction Conditions

Temperature115 °C

Reaction Steps

To a suspension of 7-(benzyloxy)-4-chloroquinoline (10 g, 37.1 mmol) and 4-nitrophenol (6.2 g, 44.5 mmol) in toluene (10 mL) was added DIPEA (6.2 g, 48.2 mmol). The reaction mixture was refluxed at 115° C. for 12 hours, then cooled down to room temperature. DCM (50 mL) was added to the mixture, and the resulted solution was washed with 1 M NaOH (30 mL each) several times till the water phase was colorless. The organic phase was concentrated in vacuo to afford a brown solid (13.2 g, 95.7%). The solid was stirred in 95% EtOH (30 mL) at room temperature for 12 hours, and filtered to give the title compound as a gray-brown solid (12.1 g, 91.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133162B2
Source datasetuspto-grants-2015_09
ORD IDord-ad6b578ce7bb451393ef739e4e7c9944
Source noteuspto-grants-2015_09