関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Bromotoluene | HCID 7805 | — |
| 反応物 | Dimethyl 2-bromoterephthalate | HCID 87741 | — |
| 反応物 | HCID 178418306 | HCID 178418306 | — |
| 触媒 | Zincchloride | HCID 3007855 | — |
| 触媒 | HCID 178418751 | HCID 178418751 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | [1,1'-Biphenyl]-2,5-dicarboxylic acid, 4'-methyl-, 2,5-dimethyl ester | HCID 105655 | 85.3% |
反応手順
4-Bromotoluene (6 g) was dissolved in tetrahydrofuran (20 ml). To this solution at -78° C. under N2 was added over a ten minute period, 1.7M tBuLi (42 ml). After two hours at room temperature, the reaction mixture was cooled to 0° C. and 1M ZnCl2 (36 ml) was added over a ten minute period. After one-half hour at room temperature, bis(triphenylphosphine)nickel(II) chloride (1.32 g) was added followed by dimethyl-2-bromo-terephthalate (6 g) in tetrahydrofuran 920 ml) dropwise over a five minute period. The reaction mixture was stirred at room temperature for two hours. The tetrahydrofuran was removed under reduced pressure. The residue was treated with ethyl acetate and 1N HCl and the layers separated. The organic phase was washed with water, brine, dried over magnesium sulfate and evaporated which gave the crude product. Chromatography on silica gel using 5% hexanes/methylene chloride gave the desired product (5.33 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05356889 |
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| 出典データセット | uspto-grants-1994_10 |
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| ORD ID | ord-be81bf75d1fc4acba37136f7bcfb08e4 |
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| 出典メモ | uspto-grants-1994_10 |
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