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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471175Generated: October 26, 2026

N-bromobutanimide → 2-Bromo-1-(6-bromoquinolin-2-yl)ethanone

https://huagongshe.com/reaction/1471175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant6-Bromo-2-(1-ethoxyvinyl)quinolineHCID 58498731—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-1-(6-bromoquinolin-2-yl)ethanoneHCID 5849889960.5%

Reaction Steps

NBS (407 mg, 2.287 mmol) was added to a solution of 6-bromo-2-(1-ethoxyvinyl)quinoline (530 mg, 1.91 mmol) in THF (10 mL) and water (2.5 mL) and the mixture was stirred at rt for 2 h. The reaction mixture was partitioned between EtOAc and brine and the organic layer was concentrated. The crude material was purified by flash silica gel chromatography (eluted with Et2O/hexanes, gradient from 0 to 5% Et2O) to yield 2-bromo-1-(6-bromoquinolin-2-yl)ethanone (380 mg) as white solid. LC-MS retention time 3.988 min; m/z 329.84 (MH+). LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a PHENOMENEX® Luna 3u C18 2.0×50 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 0.8 mL/min, a gradient of 100% Solvent A/0% Solvent B to 0% Solvent A/100% Solvent B, a gradient time of 4 min, a hold time of 1 min, and an analysis time of 5 min where Solvent A was 10% MeOH/90% H2O/0.1% trifluoroacetic acid and Solvent B was 10% H2O/90% MeOH/0.1% trifluoroacetic acid. MS data was determined using a MICROMASS® Platform for LC in electrospray mode.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006455B2
Source datasetuspto-grants-2015_04
ORD IDord-b7fdcc0dae6148bfae6df99fe8f51644
Source noteuspto-grants-2015_04