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HRID 47178Erstellt: 23. Oktober 2026

1,2-Dibromoethane → 3,3'',5,5''-Tetra-naphthyl-p-quaterphenyl

https://huagongshe.com/de/reaction/47178

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DibromoethaneHCID 7839—
Edukt4,4'-Diiodo-1,1'-biphenylHCID 76348—
EduktMagnesiumHCID 5462224—
Edukt1,1'-(5-Bromo-1,3-phenylene)dinaphthaleneHCID 22743684—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3,3'',5,5''-Tetra-naphthyl-p-quaterphenylHCID 2274368681%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A solution of 3,5-di-α-naphthyl bromobenzene (10.0 g, 0.0244 mol) in anhydrous THF (70 mL) was added dropwise to magnesium turnings (0.59 g, 0.0244 mol) in 10 mL THF. The solution was heated at 60° C. during the addition and the reaction was initiated using 1,2-dibromoethane. After the addition was complete, the brown solution was heated at reflux for 2 hrs. and then cooled to room temperature. In a separate flask, 4,4′-diiodobiphenyl (3.3 g 0.008 mol) and 0.3 g of dichlorobis(triphenyl phosphine)palladium(II) were placed under nitrogen and 30 mL of anhydrous THF was added. The Grignard reagent prepared about THF solution was then added using needle-transfer and an orange solution resulted. Heat was applied and the solution turned to almost black. The mixture was then heated at reflux for 45 min. and cooled to room temperature during which time a solid precipitated out of solution. A 2.0 M solution of HCl was added to the mixture and after stirring for 30 minutes, the water layer was removed. The solid precipitate was collected by filtration and washed with water and diethyl ether to yield a white solid (5.3 g, 81%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699595B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-12c65c39c56a4a428c86722dd8dd49d5
Quellennotizuspto-grants-2004_03