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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194434Generated: November 1, 2026

p-Chlorophenacyl bromide → 1-(p-Chlorophenacyl)-3-[[p-(dimethylamino)benzylidene]amino]-2-(p-methoxyphenyl)imidazolium bromide

https://huagongshe.com/reaction/1194434

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Chlorophenacyl bromideHCID 68303—
ReactantHCID 54562755HCID 54562755—
SolventAcetonitrileHCID 6342—
Product1-(p-Chlorophenacyl)-3-[[p-(dimethylamino)benzylidene]amino]-2-(p-methoxyphenyl)imidazolium bromideHCID 70361176—

Reaction Steps

0.93 g of p-chlorophenacyl bromide is added to a solution of 0.64 g of 1-[[p-(dimethylamino)benzylidene]amino]-2-(p-methoxyphenyl)imidazole in 20 ml of acetonitrile. After stirring at 60° for 6 hours, the mixture is left to stand for 16 hours and the product is removed by filtration and washed with ether. There is obtained 1-(p-chlorophenacyl)-3-[[p-(dimethylamino)benzylidene]amino]-2-(p-methoxyphenyl)imidazolium bromide of melting point 242°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04814332
Source datasetuspto-grants-1989_03
ORD IDord-284e907d69e14811941bfefadfa28716
Source noteuspto-grants-1989_03