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Sodium Iodide → N-Methyl-N-(5-nitrobenzofur-2-ylmethyl)-4-nitrophenethylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | N-methyl-4-nitrophenethylamine | HCID 2794239 | — |
| 反応物 | 2-(Bromomethyl)-5-nitro-1-benzofuran | HCID 11414179 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-Methyl-N-(5-nitrobenzofur-2-ylmethyl)-4-nitrophenethylamine | HCID 15735404 | — |
反応手順
N-Methyl-4-nitrophenethylamine (0.41 g, 2.3 mmole), 2-bromomethyl-5-nitrobenzofuran (0.66 g, 2.6 mmole), sodium iodide (0.39 g, 2.6 mmole) and potassium carbonate (0.36 g, 2.6 mmole) were heated at reflux temperature in acetonitrile (50 ml) for 8 days. The solvent was then evaporated, water was added, and the mixture extracted three times with methylene chloride. The combined organic extracts were washed with water, dried (MgSO4) and evaporated to give a semi-solid which was recrystallised from isopropanol to give the title compound, yield 380 mg.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05158964 |
| 出典データセット | uspto-grants-1992_10 |
| ORD ID | ord-ad3a2c54629f43b28311db2f18ad79eb |
| 出典メモ | uspto-grants-1992_10 |