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 | 5-Bromo-1,3-difluoro-2-[(octan-2-yl)oxy]benzene | HCID 68499982 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 3,5-Difluoro-4-(1-methylheptyloxy)phenylboronic acid | HCID 68499248 | — |
反応手順
14.5 g of 1-bromo-3,5-difluoro-4-(1-methylheptyloxy)benzene from step 1 were dissolved in 150 ml of diethyl ether and cooled to −70° C. At this temperature, with cooling, firstly 31.0 ml of a 15% solution of butyllithium in n-hexane were slowly added dropwise, the mixture was stirred at the same temperature for 1 h, and then 5.6 ml of trimethyl borate were slowly added dropwise, and the mixture was stirred for a further h. The temperature of the reaction solution was slowly allowed to rise to −10° C. The mixture was then hydrolysed with distilled water, and the pH was adjusted to 2 using hydrochloric acid. The organic phase was separated off, and the aqueous phase was extracted with MTB ether. The product was subjected to conventional purification and dried over Na2SO4, giving 13.9 g of 3,5-difluoro-4-(1-methylheptyloxy)phenylboronic acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07790929B2 |
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| 出典データセット | uspto-grants-2010_09 |
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| ORD ID | ord-5af2f04a350c4adaabb2df1cab296330 |
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| 出典メモ | uspto-grants-2010_09 |
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