HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tetrahydrofuran → 3,3',3''-(benzene-1,3,5-triyltris(methylene))tris(4,5-dichloro-1-(naphthalen-1-ylmethyl)-1H-imidazol-3-ium) bromide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 1-(Bromomethyl)naphthalene | HCID 137844 | — |
| Edukt | 4,5-Dichloroimidazole | HCID 140018 | — |
| Edukt | 1,3,5-Tris(bromomethyl)benzene | HCID 530258 | — |
| Produkt | 3,3',3''-(benzene-1,3,5-triyltris(methylene))tris(4,5-dichloro-1-(naphthalen-1-ylmethyl)-1H-imidazol-3-ium) bromide | HCID 86719746 | — |
Reaktionsschritte
4,5-dichloroimidazole (3.00 g, 21.90 mmol) was dissolved in THF and brought to reflux. Potassium hydroxide (2.46 g, 43.80 mmol) was added to the solution and allowed to reflux for 30 min. 1,3,5-tris(bromomethyl)benzene (2.61, 7.30 mmol) was added to the solution and refluxed overnight. Solution was filtered while hot to remove the KBr precipitate and the filtrate returned to reflux. 1-(bromomethyl)naphthalene (4.84 g, 21.90 mmol) was added to the solution and refluxed for 3 h. The volatiles were removed in vacuo and the resulting waxy yellow solid was washed in ethyl ether. A resulting product will be collected and analyzed.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09278951B2 |
| Quelldatensatz | uspto-grants-2016_03 |
| ORD ID | ord-a82ad7559bce4983b97eac21cd1f30bb |
| Quellennotiz | uspto-grants-2016_03 |