HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922596Generated: October 31, 2026
Potassium Hydroxide → HCID 70982117, compound
https://huagongshe.com/reaction/922596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Reactant | 4,5-Diiodo-1H-imidazole | HCID 2773382 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70982117 | HCID 70982117 | — |
Reaction Steps
4,5-diiodoimidazole (5.0 mmol) and KOH (5.0 mmol) were placed in a round bottom flask with 50 mL THF. The mixture was brought to reflux and stirred 0.5 h until KOH was consumed. 2-bromomethylnapthalene (5.0 mmol) was added and the solution was stirred at reflux for 17 hours. KBr was removed by vacuum filtration and the filtrate was collected. The volatiles were removed by rotary evaporation to give 4,5-diiodo-1-(naphthalen-2-ylmethyl)-1H-imidazole as a off white solid. 4,5-diiodo-1-(naphthalen-2-ylmethyl)-1H-imidazole was dissolved in acetonitrile in a round bottom flask. The solution was brought to reflux and excess iodomethane was added. The reaction was stirred at reflux for overnight after which time it was cooled. The resulting yellow precipitate was collected by filtration and analyzed. 1H NMR (300 MHz, d6-DMSO): δ 3.88 (s), 5.64 (s), 7.47-7.60 (m), 7.89-8.02 (m), 9.57 (s) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278951B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-8b26ad893a4d4de0a9a4c4c657beb7f1 |
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| Source note | uspto-grants-2016_03 |
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