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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750080Generated: November 2, 2026

1,4-Dibromobutane → 7-(4-Bromobutoxy)-quinoline-2(1H)-one

https://huagongshe.com/reaction/1750080

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium CarbonateHCID 11430—
Reactant7-HydroxycarbostyrilHCID 10975787—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product7-(4-Bromobutoxy)-quinoline-2(1H)-oneHCID 1075631541.4%

Reaction Steps

A mixture of intermediate 14 (193 mg, 1.2 mmol), 1,4-dibromobutane (0.43 mL, 3.6 mmol) and anhydrous K2CO3 (166 mg, 1.2 mmol) was dissolved in EtOH and the solution was heated to reflux overnight. The solution was diluted with water and extracted with EtOAc. The combined organic layers was washed with saturated aq NaHCO3, brine, dried over anhydrous Na2SO4, concentrated in vacuo and purified by flash chromatography on silica gel column (elution with PE/EtOAc=2:1) to give 7-(4-bromobutoxy)quinolin-2(1H)-one (intermediate 15) (147 mg, 41%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156822B2
Source datasetuspto-grants-2015_10
ORD IDord-7a34e85f0b0448efa2fd470319653a82
Source noteuspto-grants-2015_10