HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 86719630, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(2-Bromoethyl)naphthalene | HCID 139541 | — |
| Reactant | 4,5-Dichloroimidazole | HCID 140018 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Product | HCID 86719630 | HCID 86719630 | — |
Reaction Steps
4,5-Dichloroimidazole (1.23 g, 9 mmol) will be dissolved into acetonitrile. Potassium hydroxide (0.61 g, 9.9 mmol) will be added and the mixture will be allowed to stir for 0.5 h. 1-bromopropane (9 mmol) will be added and the solution will be allowed to reflux overnight. The solution will be filtered hot to remove a white precipitate (presumed to be KBr) and 1-(2-bromoethyl)naphthalene (9 mmol) will be added and the mixture will be returned to reflux overnight. The mixture will be allowed to cool to room temperature, and the volatiles will be removed en vacuo resulting in the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278951B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-f67f1d0125204ed78db08d065a5cd0f2 |
| Source note | uspto-grants-2016_03 |