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Tetrahydrofuran → 1H-Indol-3-Ylmethanamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 3-Cyanoindole | HCID 230282 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 1H-Indol-3-Ylmethanamine | HCID 472107 | 54.5% |
反応手順
Lithium aluminum hydride (100 mg) was added to a solution of 1H-indole-3-carbonitrile (100 mg) in 15 mL of 2:1 dioxane:tetrahydrofuran. The mixture was refluxed for 0.5 h, then cooled to 0 C and quenched by the sequential addition of 0.1 mL water, 0.1 mL 3 N sodium hydroxide, and 0.3 mL more water. After the mixture was stirred for 15 min at rt, the aluminum salts were removed by filtration and the solvent was evaporated to give 56 mg of C-(1H-indol-3-yl)methylamine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07084154B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-51057ba33ac843df960a60de27fd9d4c |
| 出典メモ | uspto-grants-2006_08 |