참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodobenzene | HCID 11575 | — |
| 반응물 | 4-Bromopyridinium chloride | HCID 88100 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 촉매 | Zincchloride | HCID 3007855 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ammonium Chloride | HCID 25517 | — |
| 생성물 | 4-Bromo-3-phenylpyridine | HCID 2762939 | 153.7% |
반응 단계
4-bromopyridine hydrochloride (1-BA-2, 1 g, 5.14 mmol) was dissolved in 5.1 mL of THF and the resulting solution was cooled to −78° C. LDA (10.28 mL of a 1 M solution in THF) was added over 10 minutes and the reaction mixture became brown. After stirring for 30 minutes, ZnCl2 (10.3 mL of a 0.5 M solution in THF) was added over 10 minutes and the resulting mixture was stirred for 10 minutes and then allowed to warm to rt. Iodobenzene (0.229 mL, 2.06 mmol) and Pd(PPh3)4 (593 mg, 0.514 mmol) were added and the resulting mixture was stirred under reflux for 2 h. The reaction mixture was diluted with aqueous saturated ammonium chloride and extracted with ethyl acetate. The organic phase was dried over Na2SO4 and evaporated. The residue was purified by silica column (hexane:EtOAc) to give 4-bromo-3-phenylpyridine (2-BA-2, 741 mg, 62%); LCMS: 234.0 m/z (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08541418B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-d42ba659b44e41ba80009cd5ab48e771 |
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| 출처 메모 | uspto-grants-2013_09 |
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