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Hydrochloric Acid → 4-(2,2,2-Trifluoroethoxy)aniline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | 1-Nitro-4-(2,2,2-trifluoroethoxy)benzene | HCID 2775769 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-(2,2,2-Trifluoroethoxy)aniline | HCID 2777119 | 94% |
反応手順
In a nitrogen atmosphere, 30.1 g (0.14 mol) of p-(2,2,2-trifluroethoxy) nitrobenzene, 82.1 g (1.47 mol) of reduced iron, 120 ml of ethanol and 40 ml of water were placed in a three-necked flask, to which 1.4 ml of concentrated hydrochloric acid was dropped under stirring and then refluxed for one hour. After cooling to a room temperature, it was separated by filtration, and the reaction solution was poured into iced water (about 2 liter), and precipitated solids were washed with water and then dried, to obtain 24.4 g (0.13 mol) of p-(2,2,2-trifluoroethoxy) aniline as pink solids. The yield was 94% and the melting point was 69.4° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05733481 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-785e0a0408f94a47b06e9ceee5b1cfa9 |
| 出典メモ | uspto-grants-1998_03 |