참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Bromide | HCID 260 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Butyl nitrite | HCID 10996 | — |
| 반응물 | 4'-Chloro-3-methylbiphen-4-ylamine | HCID 23005188 | — |
| 촉매 | copper(I) bromide | HCID 24593 | — |
| 생성물 | 4-Bromo-4'-chloro-3-methylbiphenyl | HCID 59450516 | — |
반응 단계
4′-Chloro-3-methylbiphen-4-ylamine (16.5 g, 0.077 mol) is added to acetonitrile (140 ml) and stirred at room temperature until dissolution is complete. The reaction mixture is cooled to between −5° C. and 0° C., tent-butyl nitrite (90%, 12.4 ml, 0.093 mol) is added dropwise and the reaction mixture is maintained at between −5° C. and 0° C. for 30-40 minutes. The mixture is added slowly to a preheated (50° C.) suspension of copper (I) bromide (5.8 g, 0.04 mol) in hydrobromic acid (5.8 ml) and stirred at 50° C. for 10-15 minutes. The reaction mixture is cooled to room temperature, then poured into ice-cold water and extracted with ethyl acetate (3×300 ml). The organic extracts are washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to yield 4-bromo-4′-chloro-3-methylbiphenyl (11.5 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08895761B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-bfcdb1d490d340b3aa4b2dd6faffe227 |
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| 출처 메모 | uspto-grants-2014_11 |
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