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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982398Generated: October 25, 2026

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

https://huagongshe.com/reaction/982398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoquinolineHCID 2762756—
Reactant6-[(6-Bromohexyl)oxy]-1-hexyneHCID 21867158—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product2-[6-[(6-Bromohexyl)oxy]-1-hexynyl]quinolineHCID 1987675975.9%

Reaction Steps

A mixture of 2-bromoquinoline (3.00 g), 6-[(6-bromohexyl)oxy]-1-hexyne (3.77 g), BTPC (90 mg), copper (I) iodide (11 mg) and dicyclohexyamine (2.79 g) in acetonitrile (35 ml) was stirred at room temperature under nitrogen for 20 h. The mixture was diluted with ether (90 ml), filtered and the filtrate evaporated in vacuo to give a brown oil. Purification by FCC eluting with hexane:ether (4:1→2:1) gave the title compound as a brown oil (4.25 g), t.l.c. (hexane:ether 2:1) Rf 0.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04996218
Source datasetuspto-grants-1991_02
ORD IDord-7d8f56412161427a9ffb1e274a6caf0a
Source noteuspto-grants-1991_02