Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,10-Phenanthroline → 4,4'-Dibromo-N,N-diphenyl[1,1'-biphenyl]-2-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,10-Phenanthroline | HCID 1318 | — |
| 반응물 | Iodobenzene | HCID 11575 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 5-Bromo-2-(4-bromophenyl)aniline | HCID 4559420 | — |
| 촉매 | Cuprous chloride | HCID 62652 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4,4'-Dibromo-N,N-diphenyl[1,1'-biphenyl]-2-amine | HCID 21976317 | 835.7% |
반응 단계
4,4′-Dibromo-2-amino-1,1′-biphenyl (16.35 g, prepared according to Libman and Slack (1951) J. Chem. Soc., p. 2588), iodobenzene (26.52 g, 0.13 mol), flake potassium hydroxide (22.4 g, 0.35 mol), 1,10-phenanthroline (0.45 g), copper (I) chloride (0.25 g), and toluene (30 ml) were charged into a flask and stirred at reflux for 15 hours. The dark reaction mixture was cooled to room temperature and diluted with 200 ml of toluene. The toluene solution was washed with DI water, dried with magnesium sulfate, and evaporated. The dark residue obtained was recrystallized trice from hexane/toluene (4:1 volume) to yield 10 grams of white crystals to yield the desired monomer. 1H NMR (CDCl3): δ=6.8–7.5, multiple peaks.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07098297B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-709f53a743134d82ad7ff2bb00604b97 |
| 출처 메모 | uspto-grants-2006_08 |