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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1253379Erstellt: 26. Oktober 2026

Toluene → O-Terphenyl

https://huagongshe.com/reaction/1253379

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktSodium CarbonateHCID 10340—
KatalysatorHCID 178418397HCID 178418397—
ProduktO-TerphenylHCID 676640%

Reaktionsschritte

6.4 mmol of the dibromide (VI) and 6.4 mmol of the arylboronic acid derivative (V) (2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)pyridine) are dissolved in 25 ml of toluene. 0.4 mmol of Pd(PPh3)4 and 10 ml of a 4N solution of Na2CO3 are added, and the mixture is heated up to reflux under nitrogen. The reaction mixture is heated under reflux for 6 hours and cooled, the phases formed are separated, and the water phase is extracted with dichloromethane and dried. The solvent is removed under reduced pressure and the crude product is purified by means of a short silica gel column. After purification by column chromatography (dichloromethane/hexane, 2:1), the desired o-terphenyl derivative is obtained in from 40 to 50% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08455112B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-01f1ee677a1542aa90333940b0032771
Quellennotizuspto-grants-2013_06