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HRID 22622Erstellt: 23. Oktober 2026

Bromobenzene → N~1~,N~1~,N~5~-Triphenylnaphthalene-1,5-diamine

https://huagongshe.com/de/reaction/22622

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromobenzeneHCID 7961—
Edukt1,5-DiaminonaphthaleneHCID 16720—
EduktTris(1,1-dimethylethyl)phosphineHCID 83681—
EduktSodium t-butoxideHCID 23676156—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelO-XyleneHCID 7237—
ProduktN~1~,N~1~,N~5~-Triphenylnaphthalene-1,5-diamineHCID 2259076215%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

1,5-Diaminonaphthalene (16.0 g, 0.101 mol) was combined with bromobenzene (47.1 g, 0.300 mol), palladium diacetate (1.2 g, 0.004 mol), tri-t-butylphosphine (4 mL), sodium t-butoxide (24.0 g, 0.26 mol), and xylene (400 mL). The mixture was heated at 140° C. with magnetic stirring under a nitrogen atmosphere. After 15 h, an additional amount of palladium diacetate (0.100 g, 0.0004 mol) was added. After heating for another 6 h, an additional amount of palladium diacetate (0.100 g, 0.0004 mol) was added. After heating for another 15 h the heat was removed. After cooling to room temperature, the solid present was filtered off and the filtrate was purified by column chromatography. This afforded 6.0 g (15% yield) of N,N,N′-triphenyl-1,5-diaminonaphthalene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06849345B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-d30650a7d9c94a198aefea829969b8d9
Quellennotizuspto-grants-2005_02