関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Bromo-2-methylphenol | HCID 16896 | — |
| 反応物 | Norborna-diene | HCID 18006658 | — |
| 溶媒 | Formic Acid | HCID 284 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 4,4'-(Bicyclo[2.2.1]heptane-2,5-diyl)bis(2-methylphenol) | HCID 67605944 | 43% |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08530133B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-f91b90d3c80848908aaec333c56a1375 |
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| 出典メモ | uspto-grants-2013_09 |
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