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Dimethylformamide → N-{2-(2-ethoxyphenoxy)ethyl}-3-(4-fluorophenoxy)propylamine hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 1-(3-Chloropropoxy)-4-fluorobenzene | HCID 74391 | — |
| 反応物 | 2-(2-Ethoxyphenoxy)ethylamine | HCID 5303042 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-{2-(2-ethoxyphenoxy)ethyl}-3-(4-fluorophenoxy)propylamine hydrochloride | HCID 21451982 | — |
反応手順
A mixture of 1.9 g of 1-chloro-3-(4-fluorophenoxy)-propane, l.8 g of 2-(2-ethoxyphenoxy)ethylamine, 0.53 g of sodium carbonate and 60 ml of dimethylformamide was heated at 80°-90° C for 15 hours. After cooling, the reaction mixture was poured into water and extracted with benzene. The extract was washed with water and dried over sodium sulfate and evaporated under reduced pressure. The oily residue was dissolved in ether and treated with ethanolic hydrogen chloride under cooling. The precipitate was collected by filtration and dried to give N-{2-(2-ethoxyphenoxy)ethyl}-3-(4-fluorophenoxy)propylamine hydrochloride, M.P. 78°-82° C. Recrystallization from ethanol-benzene gave white crystals, M.P. 84°-86° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04010280 |
| 出典データセット | uspto-grants-1977_03 |
| ORD ID | ord-37fbbc9a11e1490786b08cabb9eb7699 |
| 出典メモ | uspto-grants-1977_03 |