Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2,6-Dihydroxyanthraquinone → 2,6-Bis(2-morpholinoethoxy)anthraquinone dihydrochloride
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2,6-Dihydroxyanthraquinone | HCID 6776 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Chlorobenzene | HCID 7964 | — |
| 생성물 | 2,6-Bis(2-morpholinoethoxy)anthraquinone dihydrochloride | HCID 20369770 | — |
반응 단계
This compound was prepared by the method of Example 3, with the exception that toluene was used as the reaction medium rather than chlorobenzene, from 36 g. (0.15 mole) of 2,6-dihydroxyanthraquinone, 100 g. (0.54 mole) of N-(2-chloroethyl) morpholine hydrochloride, 66g. (1.0 mole) of potassium hydroxide pellets (85%), 400 ml. of toluene and 100 ml. of water. The dihydrocholoride salt was recrystallized twice from isopropanol with enough water added to effect solution. The pure compound melted with decomposition at 288-290° C.; λmax (H2 0) 273 μ, E1cm.1% 778.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04073904 |
| 출처 데이터셋 | uspto-grants-1978_02 |
| ORD ID | ord-82cee194515f4adb839daa1a4052b408 |
| 출처 메모 | uspto-grants-1978_02 |