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Triethylamine → 1-Cyclopropyl-3,3-diphenylurea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | N,N-Diphenylcarbamic chloride | HCID 65741 | — |
| 反応物 | Cyclopropylamine | HCID 69828 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 1-Cyclopropyl-3,3-diphenylurea | HCID 23338398 | — |
反応手順
The thus formed solution of diphenylcarbamic acid chloride was then added dropwise upon stirring to a mixture of 114 g of cyclopropylamine, 202 g of triethylamine and 500 ml of toluene. During the addition the temperature inside the flask rose to 85° C. Subsequently the reaction mass was heated to boiling point for 15 minutes and then cooled. The precipitated triethylammoniumchloride was removed by suction and the solvent was distilled off in a vacuum. The remaining residue was subjected to recrystallization from diisopropylether. The yield in 1-cyclopropyl-3,3-diphenylurea was 440.2 g (87.2% of the theoretical value). The melting point was 98° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04225338 |
| 出典データセット | uspto-grants-1980_09 |
| ORD ID | ord-08cc12ef6c4d4bbda248ae4a67ac3d48 |
| 出典メモ | uspto-grants-1980_09 |