関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Trimethyl borate | HCID 8470 | — |
| 反応物 | 2'-Fluoro-2,3-dimethoxybiphenyl | HCID 57264076 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 2'-Fluoro-2,3-dimethoxybiphenyl-4-boronic acid | HCID 67775747 | 65% |
反応手順
In the atmosphere of argon, 19.7 g of 2′-fluoro-2,3-dimethoxybiphenyl and 500 mL of anhydrous THF were placed in a flask. 56 mL of a hexane solution of 1.6M n-butyllithium was added, and the reaction solution was stirred at room temperature for 4 hours. After cooling to −78° C., 30 mL of a THF solution of 27.8 g of trimethyl borate was added dropwise. While heating to room temperature, the reaction solution was stirred for 8 hours. 200 mL of 10% HCl was added to the reaction solution, and the resulting mixture was stirred for 2 hours. The reaction solution was extracted with ether. An aqueous phase was removed, and then an organic phase was washed with saturated saline. After drying the organic phase with magnesium sulfate, the organic phase was concentrated, and residues were washed with hexane, whereby 15.2 g (yield: 65%) of 2′-fluoro-2,3-dimethoxybiphenyl-4-boronic acid was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09147847B2 |
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| 出典データセット | uspto-grants-2015_09 |
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| ORD ID | ord-4d5a7cc3380a42de8b853c9cb1f749f7 |
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| 出典メモ | uspto-grants-2015_09 |
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