Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dimethylamine → 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dimethylamine | HCID 674 | — |
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | N-ethyl carbazole | HCID 6836 | — |
| 반응물 | 4-Chlorobutyryl chloride | HCID 78370 | — |
| 반응물 | Fumaric Acid | HCID 444972 | — |
| 반응물 | 3,6-Bis(4-chlorobutyryl)-N-ethylcarbazole | HCID 12331790 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole | HCID 461319 | — |
| 생성물 | Fumarate | HCID 5460307 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US03947593 |
| 출처 데이터셋 | uspto-grants-1976_03 |
| ORD ID | ord-98dbf57019ff4ad687fba3e1257f67bf |
| 출처 메모 | uspto-grants-1976_03 |