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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380360Generated: October 31, 2026

1-(4-Bromobutyl)-4-methoxybenzene → 1-Heptyl-3-[4-(4-methoxyphenyl)butyl]-2,4,5-trimethylimidazolium bromide

https://huagongshe.com/reaction/1380360

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromobutyl)-4-methoxybenzeneHCID 578191—
Reactant1-Heptyl-2,4,5-trimethyl-1H-imidazoleHCID 20188300—
SolventWaterHCID 962—
Product1-Heptyl-3-[4-(4-methoxyphenyl)butyl]-2,4,5-trimethylimidazolium bromideHCID 23182139—

Reaction Conditions

Temperature125 °C

Reaction Steps

Add 3.23 g (0.0133 mole) of 1-(4-bromobutyl)-4-methoxybenzene to 2.77 g (0.0133 mole) of 1-heptyl-2,4,5-trimethyl-1H-imidazole and heat at 125° C. for two hours. Follow the progress of the reaction by thin-layer chromatography on silica gel (methanol:1M sodium chloride, 95:5). At the completion of the reaction, dissolve the cooled reaction mixture in 100 ml water and then wash with 100 ml cyclohexane. Extract aqueous layer with 150 ml methylene chloride and evaporate to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581370
Source datasetuspto-grants-1986_04
ORD IDord-32ab124ef15448b283d7054dda17931c
Source noteuspto-grants-1986_04