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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551116Generated: October 26, 2026

Benzyl Bromide → HCID 59829697, compound

https://huagongshe.com/reaction/551116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Prop-2-enylquinolin-8-olHCID 3654918—
SolventAcetoneHCID 180—
SolventDiethyl EtherHCID 3283—
ProductHCID 59829697HCID 5982969772%

Reaction Steps

To a stirring solution of 7-allylquinolin-8-ol (14.56 mmol, 1 eq.) in acetone (50 mL) in a round bottom flask equipped with a reflux condenser was added potassium carbonate (151.94 mmol, 10.44 eq.) followed by benzyl bromide (17.47 mmol, 1.2 eq.) and the resulting solution was stirred and heated to reflux for 20 h. Additional potassium carbonate (151.94 mmol, 10.44 eq.) was added followed by additional benzyl bromide (29.12 mmol, 2 eq.) and the resulting mixture was heated at reflux and stirred 2 h. The reaction mixture was then cooled to room temperature and diluted with 50 mL of diethyl ether. The resulting suspension was filtered and the filtrate concentrated to a yellow oil that was purified by column chromatography using 10% acetone/dichloromethane to give the product as a pale yellow oil (10.48 mmol, 72%). MS (ESI) m/z 276.2; HRMS: calcd for C19H17NO+H+, 276.13829; found (ESI-FTMS, [M+H]1+), 276.13828.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947712B2
Source datasetuspto-grants-2011_05
ORD IDord-194ad1fa34004480870ae71d8abe4131
Source noteuspto-grants-2011_05