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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421530Generated: November 1, 2026

Aniline → N,9-Diphenyl-9H-carbazol-3-amine

https://huagongshe.com/reaction/421530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantO-XyleneHCID 7237—
Reactant3-Bromo-9-phenylcarbazoleHCID 18942624—
ReactantSodium t-butoxideHCID 23676156—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
Catalyst1,1`-Bis(diphenylphosphino)ferroceneHCID 15241612—
SolventTolueneHCID 1140—
ProductN,9-Diphenyl-9H-carbazol-3-amineHCID 5981595475%

Reaction Conditions

Temperature90 °C

Reaction Steps

Into a 500 mL three-neck flask were added 19 g (60 mmol) of 3-bromo-9-phenylcarbazole, 0.34 g (0.60 mmol) of bis(dibenzylideneacetone)palladium(0), 1.6 g (3.0 mmol) of 1,1-bis(diphenylphosphino)ferrocene, and 13 g (0.18 mol) of sodium tert-butoxide, and the atmosphere in the flask was substituted with nitrogen. Then, 110 mL of dehydrated xylene and 7.0 g (75 mmol) of aniline were added thereto. This was heated and stirred at 90° C. for 7.5 hours under a stream of nitrogen. After the reaction was completed, about 500 mL of hot toluene was added to the reaction solution, followed by filtration through Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135), alumina, and Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855). The obtained filtrate was concentrated, and hexane and ethyl acetate were added thereto, followed by irradiation with ultrasonic waves, whereby a solid substance was precipitated. This solid substance was collected by suction filtration and dried to produce 15 g (75% yield) of N-phenyl-(9-phenyl-9H-carbazol-3-yl)amine (abbreviation: PCA) as a milky white powder. By a nuclear magnetic resonance method (NMR), this compound was proved to be N-phenyl-(9-phenyl-9H-carbazol-3-yl)amine (abbreviation: PCA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101289B2
Source datasetuspto-grants-2012_01
ORD IDord-66d45bf979e54a8f8ec591e3b550d2f2
Source noteuspto-grants-2012_01