HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → N-2-Hydroxyethylperylene-3,4-dicarboximide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | N-(1-Hexylheptyl)perylene-3,4-dicarboximide | HCID 11443487 | — |
| Reactant | Perylene-3,4-dicarboxylic anhydride | HCID 11759069 | — |
| Product | N-2-Hydroxyethylperylene-3,4-dicarboximide | HCID 12287885 | — |
Reaction Steps
190 mg (0.56 mmol) of perylene-3,4-dicarboxylic anhydride are reacted with 0.85 ml (1.40 mmol) of 2-aminoethanol and 1.18 g of imidazole under an argon inert atmosphere for 96 h as in 2c, and the reaction product is worked up and dried in a drying cabinet. To remove unreacted starting material, it is boiled in 10 per cent potassium carbonate solution and washed with hot water until the filtrate run-off is colourless. The brown-red product is dried in a drying cabinet at 120° C. and then recrystallized by extraction with toluene. Yield 50 mg (23%), m.p. >260° C. UV (CHCl3): λmax =489 nm, 509. Fluorescence (CHCl3, exc. 489 nm) λmax (Irel =546 nm (1), 579 (sh, 0.46).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05650513 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-76d33a3060764c92855f7411bf838700 |
| Source note | uspto-grants-1997_07 |