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Ethanol → 6-Iodoindoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 1-Acetyl-6-iodoindoline | HCID 11666396 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 6-Iodoindoline | HCID 11615696 | 64% |
反応手順
1-Acetyl-6-iodoindoline (1.06 g, 3.7 mmol), NaOH (1.16 g, 29 mmol), EtOH (8 mL), and H2O (6 mL) are heated at 90° C. overnight. The reaction mixture is then partitioned between H2O and EtOAc. The organic layer is extracted into aqueous HCl. The aqueous layer is in turn basified with NaOH, and is extracted with EtOAc. The organic layer is dried and concentrated. Hexane trituration yields 6-iodoindoline (577 mg, 64%) as a brown solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07868037B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-a0f13259a14d43c5b16fbd2049ae4af8 |
| 出典メモ | uspto-grants-2011_01 |