HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dimethylamine → 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dimethylamine | HCID 674 | — |
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | N-ethyl carbazole | HCID 6836 | — |
| Edukt | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Edukt | Fumaric Acid | HCID 444972 | — |
| Edukt | 3,6-Bis(4-chlorobutyryl)-N-ethylcarbazole | HCID 12331790 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole | HCID 461319 | — |
| Produkt | Fumarate | HCID 5460307 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US03947593 |
| Quelldatensatz | uspto-grants-1976_03 |
| ORD ID | ord-98dbf57019ff4ad687fba3e1257f67bf |
| Quellennotiz | uspto-grants-1976_03 |