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Dimethylformamide → 4-Fluoro-2-nitro-1-propoxybenzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1-Iodopropane | HCID 33643 | — |
| 反応物 | 4-Fluoro-2-nitrophenol | HCID 136236 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-Fluoro-2-nitro-1-propoxybenzene | HCID 66917174 | 96.3% |
反応手順
A N,N-dimethylformamide (DMF) solution (3 ml) of potassium carbonate (3.48 g, 25.2 mmol) and 1-iodopropane (3.95 g, 23.2 mmol) was added to a DMF solution (7 ml) of 4-fluoro-2-nitrophenol (3.3 g, 21.0 mmol). The mixture was stirred at room temperature for 48 hours. Water was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride solution twice, and concentrated under reduced pressure. The residue was purified using silica gel column chromatography (n-hexane:ethyl acetate=9:1). The purified product was concentrated under reduced pressure to thereby obtain 4.03 g of oily yellow 4-fluoro-2-nitro-1-propoxybenzene (yield: 96%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09403773B2 |
| 出典データセット | uspto-grants-2016_08 |
| ORD ID | ord-04f9775f03d749c2afa0d8fc460d327a |
| 出典メモ | uspto-grants-2016_08 |