HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1,3-Bis(quinoxalin-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)quinoxaline | HCID 5287759 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,3-Bis(quinoxalin-2-ylmethyl)-4,5-dichloroimidazolium bromide | HCID 86719694 | — |
Reaction Steps
4,5-dichloroimidazole (1.37 g, 10 mmol) will be dissolved in a minimum amount of acetonitrile and potassium hydroxide (0.62 g, 11 mmol) will be added. The mixture will be stirred at reflux until the potassium hydroxide is consumed, approximately 30 min. 2-(Bromomethyl)quinoxaline (2.23 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 potassium bromide generated. A second addition of 2-(bromomethyl)quinoxaline (2.23 g, 10.0 mmol) will be made to the reaction solution, which will be returned to reflux for 6 h. Removal of the volatile components under reduced pressure should yield the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278951B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-054b5819a5b84d47a6bd73a2811a041e |
| Source note | uspto-grants-2016_03 |