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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 505848Erstellt: 27. Oktober 2026

Diphenylamine → 8,9-Dihydrocyclopenta[def]phenanthrene

https://huagongshe.com/reaction/505848

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiphenylamineHCID 11487—
EduktTris(1,1-dimethylethyl)phosphineHCID 83681—
Edukt2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthreneHCID 12524367—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkt8,9-Dihydrocyclopenta[def]phenanthreneHCID 605749—

Reaktionsschritte

The compound 2 (1 g, 1.747 mmol), diphenylamine (0.88 g, 5.241 mmol), sodium tert-butoxide (0.51 g, 0.5 mmol), Pd2(dba)3 [(tris(dibenzylidene acetone) dipalladium(0))] (0.08 g, 0.087 mmol), and tri(tert-butyl)phosphine (0.017 g, 0.087 mmol) in a 50 ml round bottom flask were dissolved with toluene (10 mL), and the reaction mixture was refluxed for 12 hours. After the reaction was terminated, the reaction solution was cooled to a room temperature and extracted with distilled water (100 ml). The combined organic layers were dried over MgSO4, concentrated, and purified by silica gel column chromatography. The eluate was concentrated and dried to give a material 1 represented by Formula 9 (10.9 g, yield: 70%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07781579B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-f07a1fcc75544d2493fb3c213b02ba6d
Quellennotizuspto-grants-2010_08