HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1,3-Bis(pyren-2-ylmethyl)-4,5-dichloroimidazolium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4,5-Dichloroimidazole | HCID 140018 | — |
| Reactant | 2-(Bromomethyl)pyrene | HCID 22613930 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,3-Bis(pyren-2-ylmethyl)-4,5-dichloroimidazolium bromide | HCID 86719710 | — |
Reaction Steps
4,5-Dichloroimidazole (0.18 g, 1.33 mmol) and potassium hydroxide (0.08 g, 1.46 mmol) will be dissolved in a minimum volume of acetonitrile and stirred at reflux for 30 min. 2-(Bromomethyl)pyrene (2.95 g, 10.0 mmol) will be added and the mixture will be returned to reflux for 3 h. The mixture will be filtered hot to remove the KBr generated. A second equivalent of 2-(bromomethyl)pyrene will be added to the filtrate and the mixture will be returned to reflux for 6 h. The volatile components will be removed under reduced pressure to yield the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278951B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-6fbbdabb0a7f4ba3bab074049af15f7a |
| Source note | uspto-grants-2016_03 |