化工社化工社 化学情報印刷レポート · 研究参考用
Ethyl Acetate → 3,5-Dichloro-4-(2,2,2-trifluoroethoxy)aniline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Stannous Chloride | HCID 24479 | — |
| 反応物 | 1,3-Dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzene | HCID 13852227 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3,5-Dichloro-4-(2,2,2-trifluoroethoxy)aniline | HCID 13852146 | 94% |
反応手順
To a solution of 1,3-dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzene (1.90 g, 6.55 mmol) in MeOH (20 mL) and 12 N HCl (20 mL) at rt, SnCl2 (3.72 g, 19.66 mmol) was slowly added to it and then the reaction mixture was stirred overnight at rt. To the reaction mixture was slowly added 3N NaOH to pH=10 and then extracted with EA. The combined organic layers were washed with brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue was purified by column chromatography over silica gel eluted with PE:EA (6:1) to provide 3,5-dichloro-4-(2,2,2-trifluoroethoxy)aniline (1.60 g, yield 94%) as pale yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08853186B2 |
| 出典データセット | uspto-grants-2014_10 |
| ORD ID | ord-ae1e0c4f0cb74bbb84f8d051cd35e0bd |
| 出典メモ | uspto-grants-2014_10 |