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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 505984Erstellt: 27. Oktober 2026

Benzene → Octylbenzene

https://huagongshe.com/reaction/505984

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
Edukt1-OcteneHCID 8125—
Edukt1-Butyl-3-methylimidazoliumHCID 2734162—
KatalysatorNickel(II) bis-triflimideHCID 131725278—
ProduktOctylbenzeneHCID 16607—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

Nickel(II) bis-triflimide (0.06 g, 0.1 mmol) was dissolved in [bmim] [NTf2] (1.0 g) in a round-bottomed flask equipped with a magnetic stirrer and reflux condenser. Benzene (3.90 g, 50 mmol) and oct-1-ene (1.12 g, 10 mmol) were added. The mixture was heated under reflux for 18 hours and was analysed by gas chromatographic analysis as in previous examples. The oct-1-ene peak disappeared and three isomers of octylbenzene were formed (70%, 20:26:54 2- to 3- to 4-isomer ratio) as well as octene dimer (30%). The less dense product phase was decanted from the ionic/catalyst phase and purified by Kugelrohr distillation. The ionic liquid and catalyst were prepared for reuse by heating at 60° C. under vacuum for 1 hour. The ionic liquid and catalyst were used for further reactions of benzene with oct-1-ene without loss of activity. This is an alkylation of benzene with an alkene using a metal bis-triflimide catalyst. Benzene and oct-1-ene react in the presence of 1% nickel(II) bis-triflimide in [bmim] [NTf2] to form three isomers of octyl benzene and a small amount of hexadecene (unknown isomeric distribution). This reaction shown below:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07781625B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-3320c7f0c0b1411f9d9c0fca4f25c737
Quellennotizuspto-grants-2010_08