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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712231Generated: November 1, 2026

Diphenylamine → HCID 23067335, compound

https://huagongshe.com/reaction/1712231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylamineHCID 11487—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantHCID 23067332HCID 23067332—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 23067335HCID 23067335—

Reaction Steps

Under an atmosphere of argon, 9-(4-chlorophenyl)-10-(4-(2,2-diphenylvinyl)phenyl)anthracene (2.4 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 suspension was refluxed for 8 hours. The reaction mixture was filtered and washed with toluene, water and methanol, and a green 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 green solid substance (2.4 g, 81%) was obtained. The result of examination of the obtained product in accordance with 1H-NMR was as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790892B2
Source datasetuspto-grants-2010_09
ORD IDord-a761b6094dcb40f4b8c0d8ffb2b4f40f
Source noteuspto-grants-2010_09