Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890854Generated: October 26, 2026

Benzene → 1-Octene

https://huagongshe.com/reaction/890854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant1-OcteneHCID 8125—
CatalystNickel(II) bis-triflimideHCID 131725278—
SolventHCID 178448536HCID 178448536—
Product1-OcteneHCID 8125—
ProductOctylbenzeneHCID 16607—

Reaction Steps

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 is shown below: The Alkylation of Benzene with oct-1-ene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06998497B2
Source datasetuspto-grants-2006_02
ORD IDord-5ef476920480468e880aab830198be04
Source noteuspto-grants-2006_02