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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982741Generated: October 25, 2026

Imidazole → 1,4-Dichloro-2-(5-iodopent-1-ynyl)benzene

https://huagongshe.com/reaction/982741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant5-(2,5-Dichlorophenyl)pent-4-yn-1-olHCID 22320759—
SolventAcetonitrileHCID 6342—
Product1,4-Dichloro-2-(5-iodopent-1-ynyl)benzeneHCID 1298894272.5%

Reaction Steps

5-(2,5-Dichlorophenyl)pent-4-yn-1-ol (13.7 g, 59.8 mmol), triphenylphosphine (20.4 g, 77.8 mmol), and imidazole (5.71 g, 83.8 mmol) in a mixed solvent (100 ml acetonitrile-150 ml ether) was stirred under nitrogen at 0° C., and to this was slowly added iodine (21.3 g, 83.8 mmol). The solution was allowed to warm to room temperature and stirring was continued for 18 hours. This was chromatographed on silica gel with hexane to give the title compound (14.7 g,72%), MS m/z 337.9 In the manner described in Example 30, above, the following alcohols in Table III were converted to the corresponding bromides:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861445B2
Source datasetuspto-grants-2005_03
ORD IDord-bf4b29bf5f514b219217fe33e405e049
Source noteuspto-grants-2005_03