Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Cycloheptylamine | HCID 2899 | — |
| Reactant | Perylene-3,4-dicarboxylic anhydride | HCID 11759069 | — |
| Product | HCID 19033234 | HCID 19033234 | — |
Reaction Steps
0.30 g (0.93 mmol) of perylene-3,4-dicarboxylic anhydride is mixed with 0.32 g (2.83 mmol) of cycloheptylamine and 3 g of imidazole, and the mixture is heated under argon at 150° C. for 4 h. The reaction product is removed from the flask by washing with ethanol, treated with 200 ml of 10% hydrochloric acid and filtered off with suction. The residue is boiled in potassium carbonate solution, filtered off with suction and washed with hot dist. water until the filtrate run-off is colourless. The product thus obtained is dried in a drying cabinet at 120° C. and then recrystallized by extraction with methanol. Yield 0.24 g (62%) of orange crystals showing a red solid fluorescence, m.p. 354°-355° C., Rf (CHCl3 /silica gel)=0.79. UV (CHCl3): λmax (ε)=505 (30370), 483 (30967), 353 (3170), 336 (3170), 295 (3460), 264 (29047). Fluorescence (CHCl3): λmax (Irel)=529 (1), 568 (0.48).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650513 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-efcc892ccb714c7f89eb99607164e449 |
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| Source note | uspto-grants-1997_07 |
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