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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2092930Erstellt: 26. Oktober 2026

1,2-Dichlorobenzene → 1,2-Bis(2-ethylhexyl)benzene

https://huagongshe.com/reaction/2092930

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichlorobenzeneHCID 7239—
EduktHCID 178443576HCID 178443576—
KatalysatorHCID 178418745HCID 178418745—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1,2-Bis(2-ethylhexyl)benzeneHCID 1592011762%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

A dry 2 L 3-neck flask with attached reflux condenser and addition funnel, flushed with dry nitrogen, was charged with 1,2-dichlorobenzene (79.4 g, 540 mmol), Ni(dppp)Cl2 (3 g, 6 mmol), and 200 mL of dry Et2O. The addition funnel was charged with 2-ethylhexylmagnesium bromide (3M, 400 mL). The solution was cooled to 5° C. and the Grignard reagent was added dropwise to the reaction. After complete addition, the reaction was stirred at 5° C. for 30 min and then warmed to room temperature (RT). The reaction was then heated to reflux for 12 h. After cooling to RT, the reaction mixture was poured onto an ice/HCl (10%) solution and extracted with MTBE. The organic fractions were dried over anhydrous MgSO4 and then concentrated. The product was purified first by distillation followed by column chromatography with hexanes, and isolated as colorless oil (101 g, 62%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08440785B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-784f089103ee4d7bbc9bafffc6e47c30
Quellennotizuspto-grants-2013_05