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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1359897Erstellt: 26. Oktober 2026

Pentacene → Pentacene maleimide

https://huagongshe.com/reaction/1359897

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPentaceneHCID 8671—
EduktMaleimideHCID 10935—
Lösungsmittel1,4-DichlorobenzeneHCID 4685—
ProduktPentacene maleimideHCID 86643198—

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

A suspension of pentacene (287 mg, 1 mmole) and maleimide (1 mmole) in 4 mL of dichlorobenzene is heated to 160° C. for 4 hours. The mixture is cooled to room temperature and the precipitate is filtered, washed with toluene and dried. Recrystallization from dichlorobenzene affords pure samples of pentacene-maleimide adduct as white needles. N-(11-bromoundecyl) maleimide-pentacene adduct (5d): Pentacene-maleimide adduct (5c) (375 mg, 1 mmole) are added to a solution of triphenyl phosphine (393 mg. 1.5 mmole) and 11-bromo-1-undecanol (375 mg, 1.5 mmole) in 40 mL of anhydrous tetrahydrofuran. To this mixture a solution of diisopropyl azodicarboxylate (300 mg, 1.5 mmole) in 10 mL of anhydrous THF is added dropwise under a stream of nitrogen. After completion of the addition, the solution is stirred at room temperature for 18 hours. The solvent is evaporated under reduced pressure and the residue is titrated with diethyl ether and the precipitate is filtered, washed with 1:1 ether-hexane and dried. Crystallization from benzene affords the pure sample of 11-bromoundecylmaleimide-pentacene adduct 5d.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07879307B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-e8304dbf10f14e2eae7256474439bdc5
Quellennotizuspto-grants-2011_02