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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1582954Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1582954

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktIodineHCID 807—
EduktTriphenylphosphineHCID 11776—
Edukt5-(2,5-Dichlorophenyl)pent-4-yn-1-olHCID 22320759—
LösungsmittelAcetonitrileHCID 6342—
Produkt1,4-Dichloro-2-(5-iodopent-1-ynyl)benzeneHCID 1298894272,5%

Reaktionsschritte

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:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06740675B2
Quelldatensatzuspto-grants-2004_05
ORD IDord-d58c9f81ad114ae2b90dbe6f42048d1a
Quellennotizuspto-grants-2004_05