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4,6-Dimethyl-2-(4-nitrophenoxy)pyrimidine → 4-((4,6-Dimethylpyrimidin-2-yl)oxy)aniline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4,6-Dimethyl-2-(4-nitrophenoxy)pyrimidine | HCID 776048 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Nickel | HCID 935 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 4-((4,6-Dimethylpyrimidin-2-yl)oxy)aniline | HCID 767037 | 95% |
反応手順
24.5 g (0.1 mole) of 2-(4-nitro-phenoxy)-4,6-dimethyl-pyrimidine were dissolved in 150 ml of dioxane and subjected to exhaustive hydrogenation with hydrogen in the presence of Raney nickel under a pressure of 50 bar at a temperature between 20° and 50° C. The catalyst was then filtered off with suction and the filtrate was evaporated under reduced pressure. 20.4 g (95% of theory) of 2-(4-amino-phenoxy)-4,6-dimethylpyrimidine were obtained in the form of a solid substance.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04627871 |
| 出典データセット | uspto-grants-1986_12 |
| ORD ID | ord-f1982e4efde24d49811c8caffc57f963 |
| 出典メモ | uspto-grants-1986_12 |