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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714760Generated: October 31, 2026

Diethyl Ether → 4-(Chloropropyl)-1-(2-quinolyl)piperazine

https://huagongshe.com/reaction/1714760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantQuipazineHCID 5011—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium HydroxideHCID 14798—
SolventAcetoneHCID 180—
Product4-(Chloropropyl)-1-(2-quinolyl)piperazineHCID 303558995%

Reaction Steps

Dissolving 853 mg of 2-piperazin-1-ylquinoline as prepared in above Step 1-1-A in 5 ml of acetone, 5 ml of an aqueous solution containing 160 mg of sodium hydroxide was added to the solution, and into which 0.5 ml of 1-bromo-3-chloropropane was dropped, followed by stirring for an overnight at room temperature. Then diethyl ether was added, followed by washing with saturated aqueous sodium hydrogencarbonate solution, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified on silica gel column chromatography (chloroform:methanol=50:1) to provide 1.10 g (95%) of 2-[4-(3-chloropropyl)piperazin-1-yl]quinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799775B2
Source datasetuspto-grants-2010_09
ORD IDord-5d76bdadd9eb4c478cc72ffa2d0d7166
Source noteuspto-grants-2010_09