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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 9,9-dibutyl-2-iodo-9H-fluorene | HCID 23072853 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 9,9-Dibutyl-n-(9,9-dibutylfluorenyl)-n-phenylfluorenamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735720B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-19dfb8e0021349e6af89e33c4f1002f8 |
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| Source note | uspto-grants-2014_05 |
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