참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Pyridiniumtribromide | HCID 21124087 | — |
| 반응물 | 1-(3-Methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanone | HCID 21985798 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 2-Bromo-1-(3-methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanone | HCID 21985688 | 59% |
반응 단계
A mixture of 1-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)ethanone (5.66 g, 22 mmol), pyridinium tribromide (10.63 g, 33.0 mmol), and glacial acetic acid (60 mL) was stirred at 110° C. for 3 h. The reaction mixture was cooled to 0-5° C., and the precipitated product was collected by filtration and washed with small amounts of water, ethanol, and diethyl ether. The crude material was purified by flash chromatography (5:95 ethyl acetate/hexane) to give 2-bromo-1-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)ethanone as a light yellow solid (4.33 g, 59% yield). HPLC ret. time 3.63 min; 1H NMR (CDCl3) δ: 2.63 (s, 3H), 2.25 (s, 2H), 7.52-7.58 (m, 2H), 7.72-7.83 (m, 3H), 8.32 (d, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07423156B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-13f279f0c2114ca1b1c429ba8eb11603 |
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| 출처 메모 | uspto-grants-2008_09 |
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