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Dimethylamine → 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylamine | HCID 674 | — |
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | N-ethyl carbazole | HCID 6836 | — |
| 反応物 | 4-Chlorobutyryl chloride | HCID 78370 | — |
| 反応物 | Fumaric Acid | HCID 444972 | — |
| 反応物 | 3,6-Bis(4-chlorobutyryl)-N-ethylcarbazole | HCID 12331790 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole | HCID 461319 | — |
| 生成物 | Fumarate | HCID 5460307 | — |
反応手順
A mixture of 15.8 g (0.039 mole) of 3,6-bis(4-chlorobutyryl)-N-ethylcarbazole, prepared from N-ethylcarbazole and 4-chlorobutyryl chloride, 75 ml of 40% aqueous dimethylamine and 2 g of potassium iodide in 175 ml of p-dioxane is heated in a reaction bomb with stirring for 44 hours. The reaction mixture is concentrated to one-half its original volume in vacuo and diluted with 500 ml of water. The semi-solid which separates is dissolved in ether and washed repeatedly with water and dried over magnesium sulfate to give the free base which is treated with fumaric acid and recrystallized from butanone to give 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole bis acid fumarate. M.P. 94°-98°C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03947593 |
| 出典データセット | uspto-grants-1976_03 |
| ORD ID | ord-98dbf57019ff4ad687fba3e1257f67bf |
| 出典メモ | uspto-grants-1976_03 |