참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Bromo-4-chloropyridine | HCID 817696 | — |
| 반응물 | 2,5-Difluoro-4-nitrophenol | HCID 2782490 | — |
| 용매 | Chlorobenzene | HCID 7964 | — |
| 생성물 | 3-Bromo-4-(2,5-difluoro-4-nitrophenoxy)pyridine | HCID 67398634 | 38% |
반응 단계
2,5-Difluoro-4-nitro-phenol (1.739 g, 9.93 mmol) and 3-bromo-4-chloro-pyridine (0.637 g, 3.31 mmol) were dissolved in chlorobenzene (6 ml) and heated at 145° C. overnight. The solvent was removed under reduced pressure and the residue partitioned between EtOAc and 10% K2CO3 (aq). The mixture was extracted with EtOAc (2×). The combined organic extracts were washed with 10% K2CO3 (aq) and brine, dried, evaporated and purified by silica gel chromatography (hexanes/EtOAc) to yield 3-bromo-4-(2,5-difluoro-4-nitrophenoxy)pyridine (414 mg, 38% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.84 (s, 1H), 8.51-8.45 (m, 2H), 7.82-7.78 (m, 1H), 7.22 (d, 1H); MS (ESI) m/z: 331.0 (M+H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08486951B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-2259fb73cd0a468bb43e968d9df6e3d5 |
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| 출처 메모 | uspto-grants-2013_07 |
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