関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 5-Hydroxyindole | HCID 16054 | — |
| 反応物 | 1-Iodo-2-methoxyethane | HCID 79136 | — |
| 反応物 | Acetone 2-methoxyethyl iodide | HCID 86634331 | — |
| 溶媒 | Toluene acetone | HCID 20247278 | — |
| 生成物 | 5-(2-methoxyethoxy)-1H-indole | HCID 10352537 | 86.2% |
反応手順
To a solution of 5-hydroxy-indole (15.2 g, 114 mmol) in 250 ml of dry acetone 2-methoxyethyl iodide (15 ml, 141 mmol, 1.25 equiv) and anhydrous K2CO3 (46.7 g, 338 mmol, 3 equiv) are added and the mixture is refluxed. Additional amounts of 0.5 equiv of 2-methoxyethyl iodide and K2CO3 are added each day. After 6 days TLC (toluene-acetone, 9:1) indicates the absence of starting material. The solid is removed by filtration, and the solvent is evaporated. The residue is taken up in dichloromethane (800 ml) and the solution is washed with 2 M aqueous HCl, 10% aqueous NaHCO3, and water. The organic layer is dried and concentrated. Column chromatography (toluene-acetone, 9:1) provides 5-(2-methoxyethoxy)-1H-indole (18.8 g, 86%). M.p. 58-60° C. (from ethyl acetate-light petroleum).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08530493B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-a397b75c02ed433587cf9bf2dbd0b0f4 |
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| 出典メモ | uspto-grants-2013_09 |
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