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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 638774Erstellt: 26. Oktober 2026

Toluene → 1,4-Phenylenebis(9,9-dimethylfluorene)

https://huagongshe.com/reaction/638774

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktSodium CarbonateHCID 10340—
Edukt1,4-Benzenediboronic acidHCID 230478—
Edukt2-iodo-9,9-dimethyl-9H-fluoreneHCID 11023630—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1,4-Phenylenebis(9,9-dimethylfluorene)HCID 86606722—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

6.94 g (21.7 mmol) of 2-iodo-9,9-dimethylfluorene and 1 g (7.25 mmol) of 1,4-phenylenebis(boronic acid) were dissolved and agitated under nitrogen flow in the mixed solvent (120 ml of degassed toluene and 60 ml of ethanol), and 145 ml of sodium carbonate solution which was prepared by dissolving 30 g of anhydrous sodium carbonate in 150 ml of water was added dropwise thereto. After agitating for 30 minutes, 840 mg (0.727 mmol) of tetrakis(triphenylphosphine) palladium was added. Heating with agitation was carried out on the oil bath heated at 80° C. for about 3 hours. After cooling the reaction solution to room temperature, 50 ml of water and 50 ml of ethyl acetate were added, the aqueous layer and the organic layer were separated, the aqueous layer was further extracted with toluene and ethyl acetate, and the extract combined with the above organic layer was dried over magnesium sulfate. The solvent was evaporated, the residual substance was refined by silica gel column chromatography (toluene:hexane=1:2), and 3.02 g of 1,4-phenylenebis(9,9-dimethylfluorene) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07691491B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-bf3eff5b1cc24aa6936fc31ffe04ca19
Quellennotizuspto-grants-2010_04