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2-Nitropropane → 3-(2-methyl-2-nitropropyl)-1H-indole-4-carboxylic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Nitropropane | HCID 398 | — |
| 反応物 | Dimethyl Sulfate | HCID 6497 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | 3-dimethylaminomethyl-1H-indole-4-carboxylic acid methyl ester hydroiodide | HCID 69518011 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | Ammonium Chloride | HCID 25517 | — |
| 生成物 | 3-(2-methyl-2-nitropropyl)-1H-indole-4-carboxylic acid methyl ester | HCID 69518095 | — |
反応手順
A 0° C. solution of 3-dimethylaminomethyl-1H-indole-4-carboxylic acid methyl ester hydroiodide (19 g, 52.7 mmol) in 75 ml of methanol and 75 ml of 2-nitropropane is treated with dimethyl sulfate (10 ml, 105.5 mmol) and solid sodium methoxide (6.3 g, 110.6.mmol) sequentially. The resulting mixture is allowed to warm to ambient temperature, and, after stirring overnight, the reaction mixture is diluted with ethyl acetate (300 ml) and saturated aqueous NH4Cl solution (500 ml). The aqueous layer is extracted with ethyl acetate (200 ml), and the combined organic layers are dried over Na2SO4 and concentrated in vacuo to give 3-(2-methyl-2-nitropropyl)-1H-indole-4-carboxylic acid methyl ester in quantitative yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07087635B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-4866853a2f2646d1ab550d48cec29d92 |
| 出典メモ | uspto-grants-2006_08 |