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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2269729Erstellt: 23. Oktober 2026

Triphenylphosphine → 4-(2-Bromoethyl)-1,1'-biphenyl

https://huagongshe.com/de/reaction/2269729

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktBromineHCID 24408—
Edukt2-[1,1'-Biphenyl]-4-yl-1-ethanolHCID 6424577—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-(2-Bromoethyl)-1,1'-biphenylHCID 6424581—

Reaktionsschritte

Bromine (1.5 ml) was added dropwise to an acetonitrile (60 ml) solution of triphenylphosphine (5 g). After stirring for 5 minutes, an acetonitrile solution (30 ml) of 2-(4-biphenylyl)ethanol (5 g) was added to the reaction mixture. The reaction mixture was stirred at room temperature for one hour and concentrated. Diethyl ether was added to the residue. The supernatant was collected, then dried and concentrated. The residue was purified by silica gel column chromatography (eluent: IPE) to obtain 2-(4-bipenylyl)ethylbromide(6 g). 2-(4-Bipenylyl)ethyl bromide (6 g) was dissolved in methanol (100 ml), which was stirred at 70° C. for 48 hours together with potassium thiocyanate (4.0 g). The reaction mixture was concentrated, and the residue was extracted with ethyl acetate. The organic layer was washed with water, then dried and concentrated. The residue was recrystallized from ethyl acetate-hexane to obtain the entitled compound (4.1 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06329389B1
Quelldatensatzuspto-grants-2001_12
ORD IDord-144927d33aa04b4aac1a23944a2acebe
Quellennotizuspto-grants-2001_12