参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 盐酸 | HCID 313 | — |
| 反应物 | 硼酸三异丙酯 | HCID 21531 | — |
| 反应物 | 4-溴环丙基苯 | HCID 12221355 | — |
| 溶剂 | 甲苯 | HCID 1140 | — |
| 溶剂 | 四氢呋喃 | HCID 8028 | — |
| 溶剂 | 正己烷 | HCID 8058 | — |
| 产物 | 4-环丙基苯硼酸 | HCID 2849428 | — |
反应步骤
2.5 M nButyllithium in hexane (14.5 mL) is added dropwise to 1-bromo-4-cyclopropyl-benzene (5.92 g) in THF (14 mL) and toluene (50 mL) chilled to −70° C. The resultant solution is stirred at −70° C. for 30 min before triisopropyl borate (8.5 mL) is added. The solution is warmed to −20° C. and then treated with 4 M aqueous hydrochloric acid (15.5 mL). The reaction mixture is further warmed to room temperature and then the organic phase is separated. The aqueous phase is extracted with ethyl acetate and the combined organic phases are dried (sodium sulphate). The solvent is evaporated and the residue is washed with a mixture of ether and cyclohexane to give the product as a colorless solid.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07745414B2 |
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| 来源数据集 | uspto-grants-2010_06 |
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| ORD ID | ord-0ba6ce0f6e0e40739ff825ced6ba4d1c |
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| 来源说明 | uspto-grants-2010_06 |
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