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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029065Generated: October 27, 2026

Aniline → 9,9-Dibutyl-n-(9,9-dibutylfluorenyl)-n-phenylfluorenamine

https://huagongshe.com/reaction/1029065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant9,9-dibutyl-2-iodo-9H-fluoreneHCID 23072853—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
Product9,9-Dibutyl-n-(9,9-dibutylfluorenyl)-n-phenylfluorenamineHCID 68982365—

Reaction Steps

40 parts of 9,9-dibutyl-2-iodofluorene, 3.7 parts of aniline, 30 parts of potassium carbonate, 6 parts of copper powders (200 meshes), and 0.87 parts of 18-crown-6 were dissolved in 50 parts of dimethylformamide (DMF), and the obtained solution was reacted in a nitrogen atmosphere at 160° C. for 24 hours. After completion of the reaction, the reaction product was filtrated, and the filtrate was then extracted with ethyl acetate-water. The ethyl acetate phase was dried over magnesium sulfate, and the ethyl acetate was then distilled away, thereby obtaining a brown tarry substance. This brown tarry substance was separated and purified by column chromatography (hexane-ethyl acetate) to obtain 15 parts of 9,9-dibutyl-N-(9,9-dibutylfluorenyl)-N-phenylfluorenamine (the following Compound (344)) in the form of a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735720B2
Source datasetuspto-grants-2014_05
ORD IDord-19dfb8e0021349e6af89e33c4f1002f8
Source noteuspto-grants-2014_05