HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dihydroxyanthraquinone → 2,6-Bis(2-morpholinoethoxy)anthraquinone dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dihydroxyanthraquinone | HCID 6776 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 2,6-Bis(2-morpholinoethoxy)anthraquinone dihydrochloride | HCID 20369770 | — |
Reaction Steps
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 dihydrochloride salt was recrystallized twice from isopropanol with enough water added to effect solution. The pure compound melted with decomposition at 288°-290°C.; γmax (H2O) 273 mμ, E1cm1% 778.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03974186 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-2f57abf0da3543e4868a1bc045bae37f |
| Source note | uspto-grants-1976_08 |