2,2-bis[N-(2-nitrophenyl)-(4-aminophenyl)]hexafluoropropane → 2,2-bis[N-(2-aminophenyl)-(4-aminophenyl)]hexafluoropropane
반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]([C:26]2[CH:31]=[CH:30][C:29]([NH:32][C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=3[N+:39]([O-])=O)=[CH:28][CH:27]=2)([C:22]([F:25])([F:24])[F:23])[C:18]([F:21])([F:20])[F:19])=[CH:13][CH:12]=1)([O-])=O.[H][H]>C(OCC)(=O)C.[C].[Pd]>[NH2:39][C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][C:33]=1[NH:32][C:29]1[CH:28]=[CH:27][C:26]([C:17]([C:14]2[CH:15]=[CH:16][C:11]([NH:10][C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=3[NH2:1])=[CH:12][CH:13]=2)([C:22]([F:23])([F:24])[F:25])[C:18]([F:20])([F:21])[F:19])=[CH:31][CH:30]=1참가 물질
실험 절차
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%).
후처리
- customAfter that, reaction
- customwas conducted at room temperature under a hydrogen
- customfor 18 hours
- customThe obtained reaction solution
- filtrationwas filtered with cerite
- customto remove the catalyst, and ethyl acetate
- customwas removed under reduced pressure
- customThe residue was re-crystallized
출처 및 근거
- ORD 기록
- ord-496e69487e88413f89480b77dc4201d0
- 출처 데이터셋
- uspto-grants-2005_02
- 특허 번호
- US06855774B2
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