참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenyl-1-naphthylamine | HCID 7013 | — |
| 반응물 | 4,4'-Dibromobiphenyl | HCID 7110 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 촉매 | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | N-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amine | HCID 16755312 | 62% |
반응 단계
A mixture of N-phenylnaphthalen-1-amine (4.41 g, 20 mmol), 4,4′-dibromo-1,1′-biphenyl (15 g, 48 mmol), sodium tert-butoxide (4.8 g, 50 mmol) and Pd(dppf)Cl2 (0.44 g, 0.6 mmol) in anhydrous toluene (100 ml) was degassed and heated at 80° C. for 10 hours. After cooling to RT, the mixture was poured into dichloromethane (400 ml) and stirred for 30 min, then washed with brine (100 ml). The organic is collected and dried over Na2SO4, loaded on silica gel, and purified by flash column (hexanes to hexanes/ethyl acetate 90:1) to give a solid which was washed with methanol and dried under air to give a white solid 4 (5.58 g, in 62% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08426040B2 |
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| 출처 데이터셋 | uspto-grants-2013_04 |
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| ORD ID | ord-84ed204c9dde47e9afa4c74109b916e3 |
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| 출처 메모 | uspto-grants-2013_04 |
|---|
