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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446802Generated: October 29, 2026

4-Bromophenol → 2-(4-bromophenoxymethyl)quinoline

https://huagongshe.com/reaction/446802

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)quinolineHCID 20394—
Product2-(4-bromophenoxymethyl)quinolineHCID 1409760550.3%

Reaction Steps

To a stirred solution of 4-bromophenol (10 g, 0.057 mol) and 2-(chloro methyl)quinoline (15.4 g, 0.063 mol) in AcN (25 mL) was added K2CO3 (24 g, 0.17 mol). The reaction mixture was refluxed for 3 h, filtered and the filtrate was concentrated in vacuo. The residue was diluted with water and extracted with EtOAc (2×200 mL). The combined organic layers were dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to obtain 2-((4-bromophenoxy)methyl)quinoline (9 g, 50%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481534B2
Source datasetuspto-grants-2013_07
ORD IDord-c0f700be047748e1993a294bf3af7ecf
Source noteuspto-grants-2013_07