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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-bis[N-(2-nitrophenyl)-(4-aminophenyl)]hexafluoropropaneHCID 22571273—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
Product2,2-bis[N-(2-aminophenyl)-(4-aminophenyl)]hexafluoropropaneHCID 2257126894.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855774B2
Source datasetuspto-grants-2005_02
ORD IDord-496e69487e88413f89480b77dc4201d0
Source noteuspto-grants-2005_02