関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Diisobutylaluminum hydride | HCID 14487 | — |
| 反応物 | 2-Chloro-4-hydroxybenzonitrile | HCID 592797 | — |
| 生成物 | 2-Chloro-4-hydroxybenzaldehyde | HCID 185363 | — |
反応手順
After 2-chloro-4-hydroxy-benzonitrile (2 g, 0.013 mol) was dissolved in anhydrous THF (40 mL), DIBAL-H 1M hexane solution (21.7 mL, 0.032 mol) was added thereto at −78° C., and the mixture was stirred for 1 hour, and then stirred at room temperature for 2 hours. After the termination of the reaction, the reactant was added with 1M HCl at 0° C. and then extracted with EtOAc. The organic layer was separated, dried with MgSO4, and concentrated under reduced pressure to obtain the title compound, which was used in the next step without a separate purification process.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09447044B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-40264fe6f229486c8612a904a343b595 |
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| 出典メモ | uspto-grants-2016_09 |
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