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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22622Generated: October 25, 2026

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

https://huagongshe.com/reaction/22622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
Reactant1,5-DiaminonaphthaleneHCID 16720—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
ProductN~1~,N~1~,N~5~-Triphenylnaphthalene-1,5-diamineHCID 2259076215%

Reaction Conditions

Temperature140 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849345B2
Source datasetuspto-grants-2005_02
ORD IDord-d30650a7d9c94a198aefea829969b8d9
Source noteuspto-grants-2005_02