HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → N-Cyclododecylperylene-3,4-dicarboximide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Cyclododecanamine | HCID 2897 | — |
| Reactant | N-(1-Hexylheptyl)perylene-3,4-dicarboximide | HCID 11443487 | — |
| Reactant | Perylene-3,4-dicarboxylic anhydride | HCID 11759069 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-Cyclododecylperylene-3,4-dicarboximide | HCID 19033238 | — |
Reaction Steps
190 mg (0.56 mmol) of perylene-3,4-dicarboxylic anhydride are reacted with 140 mg (1.28 mmol) of cyclododecylamine and 2.0 g of imidazole under an argon inert atmosphere as in 2c, and the reaction product is worked up. After chromatography on silica gel using chloroform, it is recrystallized by extraction with toluene. Yield 190 mg (66%), m.p. 285° C., Rf (CHCl3 /silica gel)=0.58. UV (CHCl3): λmax (ε): 454 (shoulder, 19085), 484 (32630), 507 (32015). Fluorescence (CHCl3, exc. 584 nm) λmax (Irel)=538 (1), 572 (sh, 0.44).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05650513 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-03b934d9077a4d16a7cfc0328aa65356 |
| Source note | uspto-grants-1997_07 |