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Triethylamine → N-methyl-3-oxo-N-(3-phenyl-2-propene-1-yl)butyramide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Diketene | HCID 12661 | — |
| 反応物 | N-methyl-3-phenylprop-2-en-1-amine | HCID 189183 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | N-methyl-3-oxo-N-(3-phenyl-2-propene-1-yl)butyramide | HCID 53834343 | — |
反応手順
0.736 g (5.0 mmol) of methyl-(3-phenyl-2-propene-1-yl)amine, 0.386 ml (5.0 mmol) of ketene dimer and 0.07 ml (0.50 mmol) of triethylamine were heated at 70° C. under stirring in 5 ml of toluene overnight. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture. After the extraction with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by the thin-layer silica gel chromatography (ethyl acetate) to obtain the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06350762B1 |
| 出典データセット | uspto-grants-2002_02 |
| ORD ID | ord-017d1d1bc74d449d88a6fc94e654953c |
| 出典メモ | uspto-grants-2002_02 |