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Dimethylformamide → (E)-Ethyl 3-(1-methyl-1H-pyrazol-4-yl)acrylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Triethyl phosphonoacetate | HCID 13345 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 1-Methyl-1H-pyrazole-4-carbaldehyde | HCID 573117 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (E)-Ethyl 3-(1-methyl-1H-pyrazol-4-yl)acrylate | HCID 68356132 | 64.2% |
反応手順
A mixture of 1-methyl-1H-pyrazole-4-carbaldehyde (2.59 g), sodium hydride (60% in oil, 1.13 g), ethyl diethylphosphonoacetate (5.8 g) and N,N-dimethylformamide (50 ml) was stirred at room temperature for 2 hrs. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to give ethyl (2E)-3-(1-methyl-1H-pyrazol-4-yl)acrylate (2.72 g, 64%) as crystals from a fraction eluted with hexane-ethyl acetate (1:1, v/v). Recrystallization thereof from ethyl acetate-hexane gave colorless prism crystals. melting point: 43-44° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07423159B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-1bd55c209f4d461382b28eb878c6df98 |
| 出典メモ | uspto-grants-2008_09 |