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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886033Generated: November 1, 2026

1,6-Dibromohexane → 2-[3-[(6-Bromohexyl)oxy]propyl]quinoline

https://huagongshe.com/reaction/1886033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium HydroxideHCID 14798—
Reactant3-(Quinolin-2-yl)propan-1-olHCID 21806134—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-[3-[(6-Bromohexyl)oxy]propyl]quinolineHCID 19876755—

Reaction Steps

2-Quinolinepropanol (0.92 g), 50% aqueous sodium hydroxide (5 ml), 1,6-dibromohexane (5 ml) and TAB (57 mg) were vigorously stirred at 21° for 6 h. The mixture was diluted with water (25 ml) and ether (100 ml) and the organic phase dried and evaporated in vacuo. The residue was purified by FCC with hexane eluant to remove 1,6-dibromohexane. Elution with ether afforded the title compound as a yellow oil (0.88 g), t.l.c. ether Rf 0.51.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05149698
Source datasetuspto-grants-1992_09
ORD IDord-72fc97cfd6b24beeb8cfedffad248d1c
Source noteuspto-grants-1992_09