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Pyridine → N-(2,6-diisopropylphenyl)-N'-(4-tert-butylcyclohexyl)urea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 4-tert-Butylcyclohexylamine | HCID 79396 | — |
| 反応物 | 2,6-Diisopropylphenyl isocyanate | HCID 92259 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(2,6-diisopropylphenyl)-N'-(4-tert-butylcyclohexyl)urea | HCID 19935041 | 59.5% |
反応手順
To a solution of 1.6 g of 4-tert-butylcyclohexylamine in 15 ml of dichloromethane was added a solution of 2.2 g of 2,6-diisopropylphenylisocyanate in dichloromethane dropwise in the presence of pyridine at 0° C. Thereafter the mixture was stirred for 1.5 hours at room temperature and concentrated. The residue was partitioned between isopropyl ether and water, and the organic layer was successively washed with 0.5N hydrochloric acid, water and sodium sulfate solution. The organic layer was dried over magnesium sulfate and then distilled away. The resulting residue was crystallized from ethyl acetate to give 2.2 g of N-(2,6-diisopropylphenyl)-N'-(4-tert-butylcyclohexyl)urea, melting at 270° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05420164 |
| 出典データセット | uspto-grants-1995_05 |
| ORD ID | ord-6a6b231c3e824992b74412a4122da314 |
| 出典メモ | uspto-grants-1995_05 |