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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088715Generated: October 25, 2026

2-[6-[(6-Bromohexyl)oxy]-1-hexynyl]quinoline → 2-[6-[(6-Bromohexyl)oxy]hexyl]quinoline

https://huagongshe.com/reaction/1088715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[6-[(6-Bromohexyl)oxy]-1-hexynyl]quinolineHCID 19876759—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-[6-[(6-Bromohexyl)oxy]hexyl]quinolineHCID 2216173773.5%

Reaction Steps

A solution of 2-[6-[(6-bromohexyl)oxy]-1-hexynyl]quinoline (2.29 g) in ethanol (120 ml) was hydrogenated at room temperature and pressure over pre-reduced 10% palladium on carbon (1 g) for 20 min. The catalyst was removed by filtration through hyflo and the filtrate evaporated in vacuo to a brown oil. Purification by FCC eluting with hexane-ether (2:1) gave the title compound as a pale brown oil (1.70 g), t.l.c. (hexane:ether 2:1) Rf 0.21.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963564
Source datasetuspto-grants-1990_10
ORD IDord-76eac424e8314a9f9f41d04ae64f749b
Source noteuspto-grants-1990_10