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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361741Generated: October 30, 2026

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

https://huagongshe.com/reaction/1361741

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, 340 mg (0.6 mmol) of bis(dibenzylideneacetone)palladium(0), 1.6 g (3.0 mmol) of 1,1-bis(diphenylphosphino)ferrocene, and 13 g (180 mmol) of sodium-tert-butoxide, and the atmosphere in the flask was substituted by nitrogen. Thereafter, 110 mL of dehydrated xylene and 7.0 g (75 mmol) of aniline were added to the mixture. This mixture was heated and stirred at 90° C. for 7.5 hours under nitrogen. After the reaction was completed, about 500 mL of hot toluene was added to the reacted mixture, and this mixture was filtered through Florisil, alumina, and celite. An oily substance was obtained by concentration of the filtrate, and hexane and ethyl acetate were added to the substance, which was followed by irradiation with ultrasound. A solid precipitated was collected by suction filtration and dried to give 15 g (75% yield) of N-phenyl-(9-phenyl-9H-carbazol-3-yl)amine (abbreviation: PCA) as cream colored powder. By a nuclear magnetic resonance measurement (NMR), it was confirmed that this compound was N,9-diphenyl-9H-carbazol-3-amine (abbreviation: PCA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880019B2
Source datasetuspto-grants-2011_02
ORD IDord-f5f862fc256d4edc8fcdc94c4fb81d6f
Source noteuspto-grants-2011_02