참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Bromo-2-methylphenol | HCID 16896 | — |
| 반응물 | Norborna-diene | HCID 18006658 | — |
| 용매 | Formic Acid | HCID 284 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4,4'-(Bicyclo[2.2.1]heptane-2,5-diyl)bis(2-methylphenol) | HCID 67605944 | 43% |
반응 단계
4-Bromo-2-methylphenol (2.03 grams, 10.8 mmol), (tris-o-tolylphosphine)2PdCl2 (0.0422 gram, 0.0537 mmol), and norbornadiene (0.257 gram, 2.79 mmol) were charged to an appropriately sized and equipped reaction vessel under nitrogen. DMF (36 mL), triethylamine and formic acid were added to what was observed to be a yellow suspension. The mixture was then heated to 75° C. in an oil bath. Upon such heating, the reaction mixture became a yellow solution, black particles appeared and a very slow evolution of gas was observed. The reaction mixture was stirred overnight at this temperature. After cooling, the reaction mixture was diluted with ethyl acetate and washed with water. The organic layer was separated and dried over anhydrous MgSO4. PP308-2, 5, (4,4′-(Bicyclo[2.2.1]heptane-2,5-diyl)bis(2-methylphenol)) was confirmed by GC-MS of the crude product (43% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08530133B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-f91b90d3c80848908aaec333c56a1375 |
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| 출처 메모 | uspto-grants-2013_09 |
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