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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47177Erstellt: 24. Oktober 2026

Iodine → 1,2,4,5-Tetra-p-biphenylylbenzene

https://huagongshe.com/de/reaction/47177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktHexabromobenzeneHCID 6905—
Edukt4-BromobiphenylHCID 7101—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1,2,4,5-Tetra-p-biphenylylbenzeneHCID 59789064—

Reaktionsschritte

Dry Mg turnings (3.9 g, 0.16 mol) and 30 mL of anhydrous THF were added to a 1 L 3-necked round-bottomed flask equipped with a condenser, a nitrogen inlet, an additional funnel and a magnetic stirring bar. 4-Bromobiphenyl (37.2 g, 0.16 mol) was dissolved in 150 mL of THF and placed in an additional funnel. The reaction flask was placed in a 50° C. oil bath and one crystal of iodine was added. Once the reaction started 4-bromobiphenyl was added dropwise to the reaction. After addition, the brownish reaction was heated at reflux for another hour and then cooled to room temperature. A suspension of hexabromobenzene (11.0 g, 0.02 mol) in 150 mL of THF was added dropwise from an additional funnel to the reaction and the mixture was stirred at room temperature overnight. The reaction was quenched with ice and 8% hydrochloric acid and extracted with 400 mL of methylene chloride. The organic layer was washed with saturated sodium chloride solution and dried over magnesium sulfate. Solvent was evaporated and the crude product was washed with hexane and filtered to give pure product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699595B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-ad8944896cb04313830eca833a323b67
Quellennotizuspto-grants-2004_03