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Water → 2,6-Dimethyl-4-[3-(methylamino)-4-nitrophenoxy]aniline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | 4-Amino-3,5-dimethylphenol | HCID 76543 | — |
| 反応物 | 5-chloro-N-methyl-2-nitroaniline | HCID 258041 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | 2,6-Dimethyl-4-[3-(methylamino)-4-nitrophenoxy]aniline | HCID 66701665 | 80.7% |
反応手順
To a solution of N-(5-chloro-2-nitrophenyl)-N-methylamine (4.0 g) in N,N-dimethylacetamide (56 ml) were added 4-amino-3,5-dimethylphenol (2.9 g) and potassium t-butoxide (2.9 g) with stirring under ice-cooling, and the resulting mixture was stirred at 75-80° C. for 1 hour. After stirring, water (74 ml) was added to the reaction mixture, and the resulting mixture was cooled gradually to room temperature. The crystals precipitated were collected by filtration and dried in vacuo to afford the title compound (4.9 g, yield: 80%) as a yellow crystalline solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07816552B2 |
| 出典データセット | uspto-grants-2010_10 |
| ORD ID | ord-da70b34ff0ce4a6d8325fae3255f7cc5 |
| 出典メモ | uspto-grants-2010_10 |