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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11742Erstellt: 24. Oktober 2026

Carbazole → 9-(10-Bromodecyl)-9H-carbazole

https://huagongshe.com/de/reaction/11742

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbazoleHCID 6854—
EduktSodium hydrideHCID 24758—
Edukt1,1-DibromodecaneHCID 11087877—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt9-(10-Bromodecyl)-9H-carbazoleHCID 21976310—

Reaktionsschritte

10 g (0.25 mol) sodium hydride (60%) was added in several portions into a solution of 30.6 g (0.20 mol) carbazole in 200 mL THF. Then the mixture was transferred into a funnel from which it was added dropwisely into a solution of 180 g (0.6 mol) dibromodecane in 500 mL THF at 70° C. and the mixture was refluxed for 48 h. After cooling, it was filtered. The filtrate was distilled in order to remove remaining dibromodecane. The residue was diluted with water and extracted with CH2Cl2. The organics was washed with brine and dried over anhydrous MgSO4 overnight. After removed the solvent by rotary evaporator, it was purified by silica chromography to give 31.6 g (41%, yield, mp 38˜40° C.) white solid product. 1H NMR (500 MHz, CDCl3), δ (ppm): 8.14 (2H, d), 7.51 (2H, d), 7.44 (2H, d), 7.26 (2H, d), 4.30 (2H, t), 3.41 (2H, t), 1.27˜1.90 (16H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098295B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-fd7d25416553452abaa8a1d4cd2d080e
Quellennotizuspto-grants-2006_08