HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23972Generated: October 28, 2026
2,2-bis[N-(2-nitrophenyl)-(4-aminophenyl)]hexafluoropropane → 2,2-bis[N-(2-aminophenyl)-(4-aminophenyl)]hexafluoropropane
https://huagongshe.com/reaction/23972
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2-bis[N-(2-nitrophenyl)-(4-aminophenyl)]hexafluoropropane | HCID 22571273 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,2-bis[N-(2-aminophenyl)-(4-aminophenyl)]hexafluoropropane | HCID 22571268 | 94.9% |
Reaction Steps
20 g (34.7 mmol) of 2,2-bis[N-(2-nitrophenyl)-(4-aminophenyl)]hexafluoropropane synthesized above were dissolved in 200 ml of ethyl acetate. Thereto was added 1 g of 10% palladium carbon as a catalyst, and replacement with hydrogen was then carried out. After that, reaction was conducted at room temperature under a hydrogen pressure of 1.01 MPa (10 atm) for 18 hours with stirring vigorously. The obtained reaction solution was filtered with cerite to remove the catalyst, and ethyl acetate was removed under reduced pressure. The residue was re-crystallized by using a chloroform-hexane mixed solution, and ethanol-water mixed solution to obtain 17 g of 2,2-bis[N-(2-aminophenyl)-(4-aminophenyl)]hexafluoropropane (hereinafter pNPN-AF) in white solid (yeild: 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06855774B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-496e69487e88413f89480b77dc4201d0 |
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| Source note | uspto-grants-2005_02 |
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