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HRID 890855作成日:2026年10月24日

Benzene → Octylbenzene

https://huagongshe.com/ja/reaction/890855

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物1-OcteneHCID 8125—
触媒Nickel(II) bis-triflimideHCID 131725278—
溶媒HCID 178448536HCID 178448536—
生成物OctylbenzeneHCID 16607—

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06998497B2
出典データセットuspto-grants-2006_02
ORD IDord-003264d5ccdd440f95a8a86847058a0d
出典メモuspto-grants-2006_02