참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Azobisisobutyronitrile | HCID 6547 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | 2-Fluoro-6-methylnaphthalene | HCID 2727845 | — |
| 용매 | Carbon Tetrachloride | HCID 5943 | — |
| 생성물 | 2-(Bromomethyl)-6-fluoronaphthalene | HCID 594633 | — |
반응 단계
To a solution of 2-fluoro-6-methylnaphthalene (0.750 g, 4.68 mmol) in carbon tetrachloride (20 mL) was added NBS (0.917 g, 5.15 mmol) and bromine (0.265 mL, 5.15 mmol) followed by AIBN (0.077 g, 0.47 mmol). The reaction mixture was heated to 70° C. and allowed to stir for 4 hours. It was then cooled to room temperature, partitioned between water and EtOAc, and the aqueous layer was extracted three times with EtOAc. The combined organic layers were dried over sodium sulfate, filtered, concentrated in vacuo and subjected to silica gel chromatography eluting with 5-50% EtOAc in hexanes to yield 2-(bromomethyl)-6-fluoronaphthalene.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08436016B2 |
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| 출처 데이터셋 | uspto-grants-2013_05 |
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| ORD ID | ord-b365ea986416468aa8a4aa4724bbbe8a |
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| 출처 메모 | uspto-grants-2013_05 |
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