化工社化工社 化学情報印刷レポート · 研究参考用
Hydrochloric Acid → 2-(3-Chloro-2,2,3-trifluoropropionamido)-5-[2-(2,4-di-tert-pentylphenoxy)-butyramido]-phenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Quinoline | HCID 7047 | — |
| 反応物 | 2-(2,4-Bis(1,1-dimethylpropyl)phenoxy)butyryl chloride | HCID 170393 | — |
| 反応物 | 2-(3-Chloro-2,2,3-trifluoropropionamido)-5-aminophenol | HCID 20531324 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 2-(3-Chloro-2,2,3-trifluoropropionamido)-5-[2-(2,4-di-tert-pentylphenoxy)-butyramido]-phenol | HCID 20531321 | — |
反応手順
A solution of 33.85 g (0.1 mole) of 2-(2,4-di-tert-pentylphenoxy)butyryl chloride in 80 ml of dioxan was added to a solution of 26.85 g (0.1 mole) of 2-(3-chloro-2,2,3-trifluoropropionamido)-5-aminophenol and 23.7 ml (0.2 mole) of quinoline in 500 ml of dioxan at room temperature. The mixture was stirred for 90 minutes and left standing overnight. Next it was poured out in 2 l of icewater and 100 ml of concentrated hydrochloric acid. The sticky residue was extracted with ether, rinsed with water until free from acid, and dried. The solvent was evaporated and the residue recrystallized from hexane.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04341864 |
| 出典データセット | uspto-grants-1982_07 |
| ORD ID | ord-a5866f60b69b4438a7eb715e4469aa46 |
| 出典メモ | uspto-grants-1982_07 |