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Iodoethane → Ethyl 2-(furan-2-yl)acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Iodoethane | HCID 6340 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Furan-2-acetic acid | HCID 75974 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Ethyl 2-(furan-2-yl)acetate | HCID 11252124 | 56.1% |
反応手順
24.8 g of 2-(furan-2-yl)acetic acid was dissolved in 590 mL of N,N-dimethylformamide and mixed with 32.6 g (0.236 mol) of potassium carbonate and 6.42 g (19.7 mmol) cesium carbonate successively. The reaction mixture was further mixed with 19 mL (0.24 mol) of iodoethane under cooling with ice and stirred at room temperature for 14 hours. After completion of the reaction, the reaction mixture was diluted with distilled water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to give 17.0 g of the desired product as a brown liquid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08658686B2 |
| 出典データセット | uspto-grants-2014_02 |
| ORD ID | ord-0fe3831f7f244a61a0c90d4c3f6ea78b |
| 出典メモ | uspto-grants-2014_02 |