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O-Phenylenediamine → 1-(4-Cyano-phenyl)-3-[-(1-phenyl-ethylamino)-phenyl]-urea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | O-Phenylenediamine | HCID 7243 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | (1-Bromoethyl)benzene | HCID 11454 | — |
| 反応物 | 4-Cyanophenyl isocyanate | HCID 170380 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-(4-Cyano-phenyl)-3-[-(1-phenyl-ethylamino)-phenyl]-urea | HCID 12043969 | — |
反応手順
1.16 g (10.8 mmol) 1,2-phenylene diamine was dissolved in 10 ml dimethyl formamide, 2.1 g (15 mmol) potassium carbonate and 1.47 ml (10.8 mmol) 1-bromo-1-phenylethane were added with stirring. After 8 hours (h) at rt, most of the starting materials were consumed. Potassium bromide was filtered off, the solvent removed, the mixture redissolved in 20 ml THF and then 1,15 g (8 mmol) 4-cyanophenylisocyanate were slowly added and stirred for another 50 h at rt. The mixture was worked up by filtration, evaporated to dryness, dissolved in ethyl acetate and washed with diluted HCl, sodium carbonate solution and brine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06706715B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-76d8bb49b18e460c92fe6379f655d37e |
| 出典メモ | uspto-grants-2004_03 |