2,6-Dibromoanthraquinone → 2,6-Dibromo-9,10-di(naphthalen-1-yl)anthracene
반응식
[C:1]1([Li])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[Br:12][C:13]1[CH:26]=[CH:25][C:24]2[C:23](=O)[C:22]3[C:17](=[CH:18][CH:19]=[C:20]([Br:28])[CH:21]=3)[C:16](=O)[C:15]=2[CH:14]=1>CCOCC.CC(O)=O>[Br:12][C:13]1[CH:26]=[CH:25][C:24]2[C:15](=[C:16]([C:9]3[C:10]4[C:5](=[CH:4][CH:3]=[CH:2][CH:1]=4)[CH:6]=[CH:7][CH:8]=3)[C:17]3[C:22]([C:23]=2[C:1]2[C:10]4[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=4)[CH:4]=[CH:3][CH:2]=2)=[CH:21][C:20]([Br:28])=[CH:19][CH:18]=3)[CH:14]=1참가 물질
반응 조건
- 온도
- 130 °C
실험 절차
5 g of 1-naphthyl lithium was dissolved in Et2O, and the resulting solution was gradually added dropwise to a solution containing 5 g of 2,6-dibromoanthraquinone dissolved in Et2O. This reaction was carried out on a dry ice bath. Then, the temperature of the reaction material was elevated to room temperature, thereby obtaining an intermediate product. The obtained intermediate product was filtered, thereby obtaining white solids. The white solids thus obtained were dissolved in 100 mL of AcOH, followed by addition of KI and NaH2PO2 and the mixture was stirred at 130° C. for 24 hours. When the reaction was complete, the reaction material was filtered with addition of water. The filtrate was recrystallized from MC and MeOH, thereby obtaining 4 g of 2,6-dibromo-9,10-di-1-naphthylanthracene.
후처리
- additionthe resulting solution was gradually added dropwise to a solution
- customThis reaction was carried out on a dry ice bath
- customwas elevated to room temperature
- customobtaining an intermediate product
- filtrationThe obtained intermediate product was filtered
- customobtaining white solids
- customThe white solids thus obtained
- filtrationthe reaction material was filtered with addition of water
- customThe filtrate was recrystallized from MC and MeOH
출처 및 근거
- ORD 기록
- ord-395eeb53d04744799182f386420a9117
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08647753B2
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