Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712232Generated: October 30, 2026

Diphenylamine → HCID 23067343, compound

https://huagongshe.com/reaction/1712232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylamineHCID 11487—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantHCID 23067338HCID 23067338—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 23067343HCID 2306734378%

Reaction Steps

Under an atmosphere of argon, 9-(4-chlorophenyl)-10-(3,4-diphenylphenyl)anthracene (2.3 g, 4.4 mmole), diphenylamine (0.9 g, 5.3 mmole, 1.2 eq), tris(dibenzylideneacetone)dipalladium(0) (0.1 g, 0.11 mmole, 5% Pd), a toluene solution of tri-t-butylphosphine (66% by weight, 0.05 ml, 0.16 mmole, 0.7 eq to Pd) and sodium t-butoxide (0.6 g, 6.3 mmole, 1.4 eq) were suspended in anhydrous toluene (20 ml). The resultant mixture was refluxed for 8 hours. The reaction mixture was filtered and washed with toluene, water and methanol, and a light yellow solid substance was obtained. The obtained solid substance was suspended in boiling toluene (40 ml). After the suspension was cooled while being left standing, the suspension was filtered, and a light yellow solid substance (2.2 g, the yield: 78%) was obtained. It was confirmed in accordance with 1H-NMR and FDMS that the obtained product was Compound (A11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790892B2
Source datasetuspto-grants-2010_09
ORD IDord-27cda8f5cc4048f0aeda421ada8600df
Source noteuspto-grants-2010_09